Name: cryo-section dissection of the adult subependymal zone for accurate and deep quantitative proteome analysis
Uploaded: 2021-10-07T15:00:00.000+00:00
Duration: 6 min 24 s
Description: Watch this Scientific Journal Video about Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis at JoVE.com

We wish to sincerely thank Mathias Mann for allowing us to perform large parts of the experiments in his laboratory, Fabian Coscia for help with LCM and proteome analysis, Tatiana Simon-Ebert for wholemount dissections, and Korbinian Mayr and Igor Paron for their technical help. We gratefully acknowledge funding from the German Research Council to MG (SFB870, TFR274), the EU (Eranet S-700982-5008-001), the ERC (aERC &#34;NeuroCentro&#34; to MG), the Swedish Society for Medical Research (SSMF, to JK) postdoctoral grant, and KI foundations and Funds (2020-01351, to JK).

All experimental procedures in this study were performed in accordance with German and European Union guidelines and were approved by the institutional animal care committee and the government of upper Bavaria (Regierung von Oberbayern). Only male C57Bl6 mice between the ages of 8-10 weeks were used for the experiments.
1. Preparation of the mouse brain (~ 15 min per mouse)
<ol>
	<li>Prepare the dissection medium by adding 5 mL of 1 M HEPES (final concentration 10 mM) to 500 mL of 1x Hank&#39;s Balanced Salt Solution (HBSS). 
	NOTE: The storage time of the dissection medium (+4 &#176;C) should not exceed 2 weeks.</li>
	<li>Sacrifice the mice by cervical dislocation and carefully dissect the brain. 
	NOTE: When investigating the ECM, the tissue should preferably be unmodified. Cervical dislocation keeps dissection time as short as possible, thereby preventing post-mortal enzymatic autodigestion as much as possible. If removal of blood is critical to the research question, simply perfuse the mouse transcardially with phosphate-buffered saline (PBS) before removing the brain.</li>
	<li>Extract the brain by manual dissection and place it in a culture dish containing ice-cold dissection medium (Figure 1B - 1). 
	NOTE: Keep the brains in dissection medium on ice throughout the dissection.</li>
	<li>Remove the olfactory bulb (OB) with a scalpel (Figure 1B - 2) by a straight coronal cut between the OB and the anterior pole of the cortex.</li>
	<li>Remove the anterior pole of the cortex with the scalpel using a coronal cut to make the lateral ventricles visible in the coronal plane (Figure 1B - 3). 
	NOTE: Make sure the coronal cut is made ~5 mm rostrally from the optic chiasm; otherwise, the rostral part of the SEZ/MEZ will be lost.</li>
	<li>Using scissors, open both lateral ventricles from the top, starting with a sagittal section from the cortical surface to the ventricular lumen, and elongate this cut in a c-shaped manner following the ventricular flexion (Figure 1B - 4).</li>
	<li>Connect the caudal ends of the left and right sagittal incision by means of an additional coronal cut with the scissors. 
	NOTE: The three cuts now form a trapezoid and will facilitate the removal of the cortex and corpus callosum in the next step.</li>
	<li>Remove the cortex and corpus callosum covering the lateral ventricles using forceps (Figure 1B - 5). Then, remove the cortex and corpus callosum that cover the medial ventricular walls. Here, make additional cuts if the tissue is attached to the medial ventricular walls, or simply lift the cortex and corpus callosum with scissors to dislodge the tissue.</li>
	<li>Carefully spread the ventricular walls with forceps (Figure 1B - 6). Remove the choroid plexus with forceps. 
	NOTE: Complete removal of the choroid plexus is important to avoid interference with the following dissection steps and avoid potential contamination of the SEZ/MEZ samples.</li>
	<li>Put the brain on a glass slide and place the glass slide on top of dry ice to freeze the brain. Maintain the ventricular walls in the open configuration. 
	NOTE: Ensure enough distance between the lateral and medial walls of the ventricle to facilitate precise and exclusive dissection of SEZ and MEZ. If the tissue contracts back into a closed configuration, use the forceps to fix the walls in the desired position during freezing. Avoid any damage to the SEZ/MEZ. Try applying minimal force, mainly at the top edge of the opened ventricles.</li>
</ol>
2. Sectioning of the prepared brain (~ 15 min per mouse)
<ol>
	<li>Cut 50-100 &#181;m thick coronal sections of the brain until the end of the lateral ventricle using a cryostat and mount the sections onto glass slides. Ensure that the brain is attached to the cryostat attachment plate at the hindbrain with OCT medium and that no OCT comes in contact with the forebrain, especially at the ventricles. 
	NOTE: OCT medium will interfere with MS measurements. However, if the tissue will be used for an antibody assay, it is unnecessary to exclude OCT medium. The use of coated glass slides is not recommended. Coated slides apply too much adhesive force on the tissue, thereby impeding the translocation of the tissue specimen from the slides into the microcentrifuge tube in the following steps.</li>
</ol>
3.&#160;Free-hand dissection of brain slices (~ 30 min per mouse)
<ol>
	<li>Place the glass slides with the brain sections on dry ice under a dissection microscope (Figure 1C - 1).</li>
	<li>Prepare the microcentrifuge tubes on dry ice, and ensure that the tubes stay on dry ice for at least 1 min to be sufficiently cold before specimen transfer. 
	NOTE: Use microcentrifuge tubes of high quality, as some low-quality tubes may shed plastic in the subsequent tissue digestion steps associated with MS measurements.</li>
	<li>Lift the slices from the dry ice for 15-30 s to achieve a brief, incomplete thawing to render the compact myelin of the striatum observable as dense white dots. 
	NOTE: Locating the border between the SEZ and the striatum becomes feasible (Figure 1C - 2, see Figure 2A for the exclusion of myelin and a comparison with the wholemount method). If thawing takes too long, the process can be accelerated by pressing a glove-covered finger onto the opposite side of the glass slide. However, this maneuver should be practiced as excessive thawing occurs easily.</li>
	<li>Separate the SEZ with a precooled scalpel from the adjacent striatum (Figure 1C,D).</li>
	<li>Transfer the SEZ either as a whole piece or sectioned into 2-4 parts into a microcentrifuge tube by using the blunt edge of the cooled scalpel. If the tissue is to be used for another type of analysis other than MS, transfer the tissue specimen into the appropriate container instead (e.g., a 96-well plate). 
	NOTE: Cutting the completely frozen tissue may lead to tissue rapidly breaking away and falling off the slide. Cutting completely thawed tissue leads to the disintegration of the tissue. Ensure that the tissue is neither completely frozen nor completely thawed.</li>
</ol>

The authors declare no competing interests

The CSD method made it possible to precisely extract SEZ tissue and generate a reliable proteome with significant depth using MS. CSD displays a clear advantage compared to wholemount dissection in terms of greatly reduced striatal contamination of SEZ samples and extracellular protein enrichment. As it is also possible to detect a similar number of proteins in individual samples (~6,500 proteins per sample) with CSD and wholemount dissection, the additional time for CSD is well worth the effort. LCM provides more precise SEZ dissection but reached a lower proteome depth, with only 3,500 proteins per sample despite using the same MS protocol as CSD (library matching and label-free quantification). Importantly, variability was much greater, probably due to the eightfold longer preparation time per sample. PCA of the samples obtained by LCM and CSD reveals a clear separation of both methods with tight region-specific clusters robustly separated from each other. In contrast, the LCM samples displayed a more scattered distribution, which is probably in part due to the length of preparation. It is unclear whether collecting far more samples over a longer period would have yielded a proteome of equal robustness and depth with LCM. Calculating an estimate, collecting a similar sample volume as done for CSD would take 5-8 times longer with LCM, even up to 15 times longer if samples provided for the peptide spectra libraries were included, and much of it under thawed conditions. Furthermore, considering the additional perturbations of the tissue necessary for LCM (background staining, laser dissection), LCM provided little, if any, gain over CSD. Hence, CSD can be deemed more suitable for extracellular proteome research, specifically for the SEZ.
Notably, if the region of interest is smaller than the SEZ (e.g., investigating only the ependymal cell layer), a free-hand approach falls behind the accuracy of the LCM. For example, using CSD to separate the ependymal from the subependymal layer is difficult as the ependymal layer is only a cell diameter wide, and the demarcation towards the subependymal layer is not visible for the naked eye in fresh frozen tissue. Hence, LCM will be a better choice than CSD if a precise dissection on a scale below 50 &#181;m is more important than undisturbed tissue or keeping the dissection time short. For regions with a width of 50 &#181;m and more, however, the precision of CSD is comparable to that of LCM for ECM protein analysis.
CSD has already proven to be useful by contributing to the investigation of the functional role of the ECM in the neurogenic niche25. Hence, the continued application of CSD in the SEZ for various protein and proteome investigations (or even single-nucleus RNA sequencing) might lead to the detection of further neurogenesis regulators, stem cell activation markers, and a deeper understanding of SEZ stem cell niche physiology. Considering the decline of neurogenesis in the aging SEZ37, a concise analysis of ECM changes of the SEZ of aged vs. young mice might promote the understanding of the exact niche mechanisms fostering NSC development and maintenance38,39. Furthermore, the influence of inflammation and injury on SEZ neurogenesis is well established40,41,42,43. The enrichment of blood-derived fibrinogen in the SEZ after cortical brain injury and its influence on SEZ astrogliogenesis and scar formation44&#160;highlights the potential influence of trauma-induced microenvironment changes on the SEZ stem cell physiology. Hence, investigating the SEZ-ECM proteome in association with brain injury using CSD could help elucidate the mechanisms by which injury and inflammation affect neurogenesis. Importantly, the method could also be applicable to human brain neurogenic niches in health and disease as fresh frozen tissue can often be obtained from surgeries. Furthermore, given the species differences in adult neurogenesis, it would also be fascinating to apply the CSD method to other species, e.g., in association to striatal neurogenesis. Moreover, with other protein detection methods, differences in locally produced growth factors can be investigated accurately and&#160;efficiently using CSD for the SEZ and MEZ (e.g., ELISA).
Lastly, the dissection procedure could potentially be modified for accurate extraction of other brain regions, also for research questions not related to neurogenesis. For instance, CSD includes a brief semi-thawing step, during which compact myelin is visible as white areas distinct from the more translucent residual brain tissue. With a simple modification of the method, this feature would allow the precise dissection of only corpus callosum compact myelin tissue, which could be subjected to proteomic analysis of injury-related changes. A suggestion of a protocol modification that would allow the corpus callous dissection is to omit steps 1.5-1.9 of the protocol and proceed directly to preparing the coronal sections instead of opening the ventricles to make the SEZ and MEZ accessible. Then, place the sections on dry ice, briefly lift and semi-thaw the slices, and simply remove the corpus callosum with a scalpel. This preparation should now be ready for any analysis requiring an efficient dissection of native corpus callosum tissue.
In summary, this study presents a micro-dissection method that could be used for reliable ventricular neurogenic niche proteome analysis. The data underline the compatibility and utility of the CSD method together with MS-based proteomic analysis of the SEZ microenvironment. The combination of precision, efficiency, and minimal tissue perturbation render the CSD a valuable extension of existing methods.

As neurogenesis is restricted in the adult brain, various central nervous system repair strategies would greatly benefit from an increased understanding of the underpinnings of adult neural replacement. Rodents have helped us understand the basic mechanisms of postnatal neurogenesis, although it should be noted that adult neurogenesis is greatly species-dependent. In mice, there are three adult neural stem cell (NSC) niches. The hypothalamus is an adult NSC niche with neurogenic potential1,2, while continuous adult neurogenesis is mainly restricted to the hippocampus3&#160;and the SEZ of the lateral walls of the lateral ventricles4,5,6. The SEZ is the largest germinal region containing NSCs (type B cells) that develop into neuroblasts (type A cells) via transit-amplifying progenitor cells (type C cells). The SEZ contains 20-35% of type B cells, 1-15% of type C cells, 1-30% of type A cells, and 25-50% of ependymal cells7. The SEZ features a complex microarchitecture, with endothelial cells, microglial cells, and ependymal cells residing in and influencing the stem cell niche8,9,10. Although neurons are scarce in the SEZ, axons emanating from distant sources such as the striatum, the ventral tegmental area, or the hypothalamus reach and influence type B cells4. A unique feature of this stem cell niche is the separation between the site of proliferation and the site of differentiation. After proliferation, the neuronal progenitors migrate several millimeters from the SEZ to the olfactory bulb, where they terminally differentiate into neurons and integrate into pre-existing neural circuits. Investigations into cell-intrinsic programs associated with neurogenesis have already provided knowledge important for experimental therapeutic cell reprogramming and transplantation strategies15,16,17,18,19,20. However, cell-extrinsic signals also regulate neurogenesis, and tissue environments can determine the neurogenic fate of stem cells11,12,14,21,22,23. Consequently, the investigation of the microenvironment of the neurogenic niches and its interaction with the stem cells is of crucial importance.
The extracellular matrix (ECM) and other secreted proteins are a large part of the microenvironment. For accurate identification and quantification, a proteomic approach is better suited than a transcriptomic approach to determine ECM composition due to the low correlation between transcriptome and protein levels for ECM24,25. Moreover, there is substantial evidence that niche regulators in the SEZ are not exclusively produced by cells populating the niche itself. More distant locations, such as the choroid plexus, secrete modulatory signals transmitted to the stem cells via the cerebrospinal fluid22,23. Investigating the niche proteome can help to identify niche regulators present in the niche independent of their production site, given that a substantial proportion of the extracellular microenvironment is assembled by proteins.
To collect the murine ventricular zone for unbiased proteomic analysis, a method with high precision is required, capturing the ca. 50 &#181;m thin paraventricular ribbon containing stem cells while excluding the tissue of the adjacent striatum. Furthermore, tissue perturbation during the dissection must be minimalized for analyzing the extracellular microenvironment because soluble proteins, including growth factors or cytokines, could be washed away easily. Although it is possible to analyze the mass spectra of fixed tissue, the required agent, such as paraformaldehyde, will reduce the protein identification depth and may introduce posttranslational modifications. A common wholemount SEZ dissection, e.g., for the collection of cells for fluorescence-activated cell sorting analysis, removes the whole SEZ with scissors26. This standard dissection is fast with minimal tissue perturbation. However, striatal contamination of the samples cannot be avoided. Conversely, LCM has the outstanding advantage of superior dissection precision. However, LCM may introduce tissue perturbations, for instance, due to background staining or laser-caused protein denaturation. To combine the strengths of the wholemount dissection and LCM, a novel method that is compatible with MS, termed cryo-section-dissection (CSD), was developed (Figure 1A-D). The CSD allows the extraction of the SEZ and the dissection of the SEZ of the medial walls of the lateral ventricles (MEZ), which is an ideal, mostly non-neurogenic control region for the SEZ (see the protocol). The niche proteome obtained by the combination of CSD and state-of-the-art MS methods proved to be useful for the characterization and identification of novel regulators in this adult NSC niche25. Hence, this method will be useful for the determination of SEZ tissue protein composition.

<table><tbody><tr><td>Cryostat CM3050S</td><td>Leica</td><td></td><td></td></tr><tr><td>Dissecting microscope</td><td>Leica</td><td></td><td></td></tr><tr><td>Dumont no. 5SF forceps, Inox super fine tip</td><td>Fine Science Tools</td><td>cat. no. 11252-00</td><td></td></tr><tr><td>Hank&amp;rsquo;s Balanced Salt Solution with CaCl&lt;sub&gt;2&lt;/sub&gt; and MgCl&lt;sub&gt;2&lt;/sub&gt;</td><td>Invitrogen</td><td>cat. no. 24020</td><td></td></tr><tr><td>HEPES buffer solution (1 M)</td><td>Invitrogen</td><td>cat. no. 15630</td><td></td></tr><tr><td>Microscope slides</td><td>RS France</td><td>cat. no. BPB018</td><td></td></tr><tr><td>Safe-lock tubes, PCR clean 2.0 mL</td><td>Eppendorf</td><td>cat. no. 0030123344</td><td></td></tr><tr><td>Spring scissors, Vannas-Tubingen 5 mm</td><td>Fine Science Tools</td><td>cat. no. 15003-08</td><td></td></tr><tr><td>Surgical disposable scalpels</td><td>B. Braun</td><td>cat. no. 5518083</td><td></td></tr><tr><td>Tissue culture dishes 60 mm</td><td>Greiner Bio-One</td><td>cat. no. 633180</td><td></td></tr><tr><td>&lt;strong&gt;Antibodies&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Alexa Fluor secondary antibodies (488, 555) (1/1,000)</td><td>ThermoFisher Scientific</td><td>cat. no. A-11001</td><td></td></tr><tr><td>DAPI</td><td>Sigma</td><td>cat. no. D9542</td><td></td></tr><tr><td>guinea pig polyclonal anti-DCX 1:500</td><td>Millipore</td><td>cat. no. AB2253,</td><td></td></tr><tr><td>mouse monoclonal anti-GFAP 1:500</td><td>Sigma</td><td>cat. no. G3893</td><td></td></tr><tr><td>mouse monoclonal anti-MAG 1:400</td><td>Millipore</td><td>cat. no. MAB1567</td><td></td></tr><tr><td>&lt;strong&gt;Software&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>GraphPad Prism version 9</td><td>GraphPad Software, San Diego California USA</td><td></td><td>www.graphpad.com</td></tr><tr><td>Perseus Version 1.6.10.50</td><td>Max-Planck Institute for Biochemistry, Munich Bavaria Germany</td><td></td><td>https://maxquant.net/perseus/</td></tr><tr><td>ZEN imaging software</td><td>Carl Zeiss</td><td></td><td></td></tr></tbody></table>

cryo-section dissection of the adult subependymal zone for accurate and deep quantitative proteome analysis

The subependymal neurogenic niche consists of a paraventricular ribbon of the lateral ventricular wall of the lateral ventricle. The subependymal zone (SEZ) is a thin and distinct region exposed to the ventricles and cerebrospinal fluid. The isolation of this niche allows the analysis of a neurogenic stem cell microenvironment. However, extraction of small tissues for proteome analysis&#160;is challenging, especially for the maintenance of considerable measurement depth and the achievement of reliable robustness. A new method termed cryo-section-dissection (CSD), combining high precision with minimal tissue perturbation, was developed to address these challenges. The method is compatible with state-of-the-art mass spectrometry (MS) methods that allow the detection of low-abundant niche regulators. This study compared the CSD and its proteome data to the method and data obtained by laser-capture-microdissection (LCM) and a standard wholemount dissection. The CSD method resulted in twice the quantification depth in less than half the preparation time compared to the LCM and simultaneously clearly outperformed the dissection precision of the wholemount dissection. Hence, CSD is a superior method for collecting the SEZ for proteome analysis.

When following the above steps, the tissue samples in the microcentrifuge tubes are ready for and compatible with MS sample preparation. After sample preparation, we obtained ~5-7 &#956;g of peptides per sample of either SEZ or MEZ per mouse. However, the final amounts of the peptides may depend on the MS preparation method. In the proteome comparisons below, protein identification and quantification depth (500-1,000 proteins per sample) were increased by computationally matching the peptide spectra to peptide spectra libraries created for each tissue region25,27. Notably, the loss-less nano fractionation method used here for the creation of the peptide spectra libraries is currently not commercially available. The raw MS data were analyzed using the MaxQuant software28, achieving mass accuracies in the parts per billion range29. The Max Quant environment allows matching between MS runs. Protein abundance was quantified using a label-free quantification algorithm30. Immunohistochemical staining was done on fresh frozen tissues and performed as previously reported25 (see the Table of Materials).
Cryo-section-dissection 
The complete SEZ and MEZ of adult mice (n = 4) were obtained using CSD (see Figure 1 and protocol). The somatosensory cortex (Cx) was dissected with surgical scissors. Additional 4 mice were dissected in the same manner; however, the dissected tissue was pooled into one sample per region to create the proteome library (10,923 identified proteins) for increased protein identification and quantification in the individual samples25. In the four individual samples, (mean &#177; SD) 6,673 &#177; 317.4 proteins were quantified in the SEZ and 6,747 &#177; 37.7 in the MEZ. All the MS proteomics data were deposited in the ProteomeXchange Consortium via the PRIDE31 partner repository, and the accession number for the proteomes reported here is ProteomeXchange: PXD016632 (http://proteomecentral.proteomexchange.org).
Comparison to wholemount dissection 
Wholemount dissection was performed according to a standard protocol26. Wholemount dissection revealed a similar number of proteins (approximately 6,000 for SEZ and 6,000 for Cx, n = 4 per group) compared to CSD25. One of the intended improvements of using CSD for the SEZ, instead of a wholemount dissection protocol, is the reduction of potential striatal contamination. In SEZ samples contaminated with tissue from another region, detected candidate proteins cannot be allocated to a region as significant enrichment can result from the region of interest and the contaminator. Immunohistochemically, the myelin-associated glycoprotein (MAG) positive myelin-rich internal capsules of the striatum were identified in the wholemount samples but seldom in the CSD samples (Figure 2A). The striatal contamination in the wholemount samples could be confirmed by identifying the enrichment of myelin proteins in the SEZ compared to the somatosensory cortex (Cx) Grey Matter (GM) samples (Figure 2B). Note that large parts of the Cx GM, especially the upper Cx layers, are unmyelinated32.
As large fiber bundles pass through the striatum, contamination by this region resulted in the enrichment of myelin proteins compared to the Cx. The myelin proteins used as markers for striatal contamination in the SEZ samples were the myelin basic protein (MBP), the myelin-associated glycoprotein (MAG), the proteolipid-protein 1 (Plp1), and the 2&#39;,3&#39;-cyclic-nucleotide 3&#39;-phosphodiesterase (Cnp). All myelin-marker proteins were significantly enriched in the SEZ compared to the Cx. Conversely, comparisons for the four myelin marker proteins in the CSD dataset yielded no significant differences when comparing SEZ to Cx (Figure 2B). Proteomic data of the striatum33 supports the hypothesis that the enrichment of myelin proteins in the SEZ samples of the wholemount dissection was caused by the contamination with striatal tissue. Hence, the CSD largely prevented contamination by striatal tissue (rich in compact myelin) compared to a wholemount dissection.
Unbiased proteome analysis of non-dissociated tissue can reveal interesting extracellular proteins. With improved dissection using the CSD, extracellular-associated proteins were significantly enriched in the samples compared to the wholemount samples (Figure 2C, annotation enrichment test). The CSD and wholemount dissection display a comparable enrichment of the gene ontology (GO) terms &#34;extracellular vesicular exosome&#34; and &#34;extracellular region part.&#34; However, the GO term &#34;Matrisome-associated&#34; is slightly more enriched in the CSD than in the wholemount dissection. Accordingly, the ECM cross-binding enzyme and recently discovered neurogenesis regulator transglutaminase-2 (Tgm2) were found enriched in the SEZ compared to Cx using the CSD25. In contrast, no difference was found between SEZ and Cx samples obtained by the wholemount dissection (Figure 2D). Proteomic data of the striatum33 support the hypothesis that the detection of the neurogenesis regulator Tgm2 by wholemount dissection was impeded by the contamination with striatal tissue. Hence, overall, the cryo-section-dissection is a successful but also necessary improvement to the standard dissection for niche-specific proteome analysis.
Comparison to Laser-capture-microscopy 
The front half of the SEZ and the MEZ of 3 adult mice were obtained for LCM (Figure 3A&#160;). Overall, the LCM method exhibits some disadvantages, specifically regarding tissue perturbation and efficiency. To visualize the region of interest under the dissection microscope, background staining is necessary, potentially washing away small or soluble proteins of interest, e.g., growth factors, cytokines, or ECM regulators such as enzymes. Furthermore, slides spend varying times at room temperature during laser removal. Moreover, the laser itself might denature proteins of interest.
CSD has a considerable advantage over LCM regarding the time and effort necessary to perform the dissection: step 1 of the protocol must be performed similarly for both CSD and LCM; without this step, ventricular walls remain adherent, making the separation of MEZ and SEZ samples difficult. Given that the CSD sections (100 &#181;m) are 6-7 times thicker than the maximum thickness34 of the LCM sections (15 &#181;m), step 2 (sectioning of the brain) and step 3 (removing the MEZ and SEZ from each coronal section) will take at least 6-7 times longer for LCM. The necessary background staining and setting up the laser microscope will consume additional time. Here, it took three times longer to harvest 50% of the SEZ and MEZ of 3 animals by LCM compared to 100% of the SEZ and MEZ of 4 animals by CSD, constituting an eightfold speed advantage of CSD. In summary, LCM not only requires a notable amount of additional effort, but the tissue is also subjected to a substantially longer period of manipulation and temperature changes that can compromise the dynamics and reliability of data generated by subsequent analysis.
The MS results of CSD were compared to the results from the laser capture microdissection (LCM). Both datasets were matched to the proteomic library generated by pooling CSD samples. On average, LCM yielded 3,441 &#177; 270.0 and 3,613 &#177; 238.7 individual proteins in the SEZ and medial ventricular zone, respectively (Figure 3B). Given the remarkable difference in protein identification, principal component analysis (PCA) displayed distinct separation according to the dissection method (component 1: 62.7%, not shown). Component 2 displayed the greatest separation for SEZ and MEZ among the LCM samples (8.5%, Figure 3C). Component 3 also seems to separate LCM and CSD; however, this difference might result from method-based differences rather than the number of identified proteins (6.4%). Nevertheless, the overall regional separation remained strikingly distinct for the cryo-dissection data and vastly better than for LCM. This discrepancy in data dynamics may result from different times spent by the specimens at room temperature during the laser dissection or a higher susceptibility of small tissue amounts to variability in the subsequent proteomics protocols and mass spectrometry measurements.
To search for differences in the proteome profile of the ECM, a 2D annotation enrichment test between CSD and LCM was performed for the SEZ and MEZ (Figure 3D). Calculating the relative enrichment of GO terms between LCM and CSD samples allows the comparison of relative proteome dynamics of the ECM protein clusters between the two methods despite the unequal amount of tissue and the differences in the dissection protocol. The plots reveal a good correlation between LCM and CSD. The annotations &#34;extracellular region part&#34; and &#34;extracellular membrane-bound organelle&#34; are similarly enriched in both methods and regions. Hence, the increased time demand of LCM does not appear to be compensated by a relatively higher sensitivity for ECM-associated proteins. Instead, CSD provides more robust identification/quantification when comparing the sample data for the neurogenesis and SEZ-associated ECM proteins Tgm2, Thrombospondin-4 (Thbs4), S100a6, and Tenacin-C (Tnc) (Figure 3E). In the case of TnC, although quantified in all samples, only CSD displayed enrichment for SEZ compared to MEZ. Nevertheless, the SEZ-associated basal membrane proteins Nidogen-1 (Nid1), Laminin subunit beta-2 (Lamb2), and basement membrane-specific heparan sulfate proteoglycan core protein (Hspg2)35&#160;displayed an even more robust enrichment in the SEZ (compared to MEZ) in the LCM samples than in the CSD samples (not shown). Hence, CSD can provide tissue samples that provide an accurate and deep quantitative proteome for SEZ characterization in a reasonable timeframe, without worrying about compromised tissue integrity or protein loss.
Statistics 
Statistical testing, 2D annotation enrichment tests, and PCA were done in the Perseus environment. Proteins were included in the analysis if a valid value was detected for each method in at least one sample. Protein abundance and number comparisons were visualized using data analysis software (see the Table of Materials). A permutation-based control of the false discovery rate (FDR) (FDR was set to 0.05, 250 randomizations) was employed for protein comparisons. For the 2D-annotation enrichment tests36, the displayed GO terms are significantly enriched (FDR was set to 0.02 using the Benjamini-Hochberg FDR-control method).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/63047/63047fig01.jpg" /> 
Figure 1: The Cryo-Section-Dissection method. (A) Overview of the region of interest: the lateral ventricle with the neurogenic SEZ and the non-neurogenic MEZ. Neuroblasts immunostained with Dcx. (B) Stepwise removal of the OB, the anterior pole, the cortex, and corpus callosum above the ventricles and the choroid plexus: 1. placement in dissection medium, 2. removal of OB, 3. removal of the anterior pole of the cortex, 4. sagittal incisions of the ventricular top, 5. removal of the ventricular top, 6. spreading of the ventricular walls. (C) 100 &#181;m coronal slices of the fresh-frozen mouse brain, (1.) before and (2.) after the removal of the ventricular walls with an ice-cold scalpel. Scale bars = 4 mm (D) Staining of a coronal section of a lateral ventricle (GFAP: green; DAPI: blue), showing the SEZ and MEZ dissected with the CSD. Scale bars = 300 &#181;m (A), 200 &#181;m (D). Abbreviations: CSD = cryo-section dissection; SEZ = subependymal zone; MEZ = medial ependymal zone; Dcx = Doublecortin; OB = olfactory bulb; GFAP = glial fibrillary acidic protein; DAPI = 4&#8242;,6-diamidino-2-phenylindole. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/63047/63047fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/63047/63047fig02.jpg" /> 
Figure 2: Superior dissection-precision with the cryo-section-dissection compared to wholemount dissection. (A) Immunohistochemical image of an SEZ sample obtained by wholemount dissection (left). The inclusion of myelin-rich striatal tissue is visualized by staining against MAG (green). Staining of a SEZ dissected with the CSD (right). In CSD, almost all the striatal myelin (staining against MAG, green) is excluded from the sample ribbon. Nuclei were visualized using DAPI (blue). (B) Comparison of myelin marker enrichment in SEZ vs. Cx from wholemount (MBP: p = 0.0074; MAG: p = 0.0016; Plp1: p = 0.0011; CNP: p = 0.0029)&#160;and CSD (MBP: p = 0.0667; MAG: p = 0.0236; Plp1: p = 0.3420; CNP: p = 0.1842). (C) 2D-annotation enrichment test comparing the wholemount-SEZ with the CSD-SEZ samples. The GO terms extracellular space and Matrisome-associated are more enriched in the CSD data than in the wholemount data. (D) The protein abundance of the NSC regulator Tgm225&#160;plotted for the wholemount dissection and the CSD. Tgm2 is significantly enriched in the SEZ compared to the Cx in CSD (CSD: p = 0.0029; Wholemount: p = 0.1775). For B and D: As reference, proteome data from Sharma et al.33 with measurements of striatum and cortex plotted for the corresponding proteins displayed in the wholemount and CSD samples. Scale bars = 200 &#181;m (A). Abbreviations: CSD = cryo-section dissection; SEZ = subependymal zone; MAG = myelin-associated glycoprotein; Cx = somatosensory cortex; MBP = myelin basic protein; Plp1 = proteolipid-protein 1; CNP = 2&#39;,3&#39;-cyclic-nucleotide 3&#39;-phosphodiesterase; GO = gene ontology; NSC = neural stem cell; Tgm2 = tranglutaminase 2; DAPI = 4&#8242;,6-diamidino-2-phenylindole; LFQ = label-free quantitation. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/63047/63047fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/63047/63047fig03.jpg" /> 
Figure 3: Improved extracellular protein quantification with cryo-section-dissection compared to LCM. (A) Cresyl violet staining of a lateral ventricle before and after laser capture of the SEZ and MEZ (left). For comparison, the CSD incision of the SEZ and MEZ (right). Scale bars = 150 &#181;m. (B) Comparison of the number of detected proteins in the SEZ and MEZ samples from CSD and LCM. Data are presented as mean &#177; SD. (C) Principal component analysis of the SEZ and MEZ samples comparing CSD and LCM (component 2: 8.5% of the variance; component 3: 6.4%). (D) 2D annotation enrichment of the cryo-section- and laser-dissected MEZ (Top) and SEZ (Bottom). The GO terms extracellular organelle and extracellular region part are significantly enriched (red dots). (E) Abundances of extracellular SEZ-associated marker proteins in SEZ and MEZ for LCM (Tnc: p = 0.3789) and the CSD samples (Tgm2: p = 0.2940; S100a6: p = 0.0218; THBS4: p = 0.3941; Tnc: p = 0.0004). Abbreviations: CSD = cryo-section dissection; LCM = laser-capture-microdissection; SEZ = subependymal zone; MEZ = medial ependymal zone; GO = gene ontology; Tnc = Tenacin-C; Tgm2 = transglutaminase 2; S100a6 = S100 calcium-binding protein A6; THBS4 = thrombospondin-4; LFQ = label-free quantitation. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/63047/63047fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis at JoVE.com

Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis

Cryo-section-dissection allows fresh, frozen preparation of the largest neurogenic niche in the murine brain for deep quantitative proteome analysis. The method is precise, efficient, and causes minimal tissue perturbation. Therefore, it is ideally suited for studying the molecular microenvironment of this niche, as well as other organs, regions, and species.

The subependymal neurogenic niche consists of a paraventricular ribbon of the lateral ventricular wall of the lateral ventricle. The subependymal zone ...

cryo-section-dissection-adult-subependymal-zone-for-accurate-deep

Nanyang Technological University

Research

JoVE Journal

Neuroscience

3.4K Views.  Ludwig Maximilian University of Munich. Onze dissectiemethode maakt een nauwkeurige isolatie van de ventriculaire neurogene niche mogelijk en is daarom zeer geschikt voor het bestuderen van de moleculaire micro-omgeving van deze niche. Het belangrijkste voordeel van deze dissectiemethode is dat het nauwkeurig en efficiënt is en minimale weefselverstoring veroorzaakt, terwijl het nog steeds compatibel is met massaspectrometrie voor proteoomanalyse. In dit protocol extraheren we de neurogene niche van de ventrikel uit een muizenbrei...

Video: Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis

Dissection of Human Retina and RPE-Choroid for Proteomic Analysis

The human retina is composed of the sensory neuroretina and the underlying retinal pigmented epithelium (RPE), which is firmly complexed to the vascular choroid layer. Different regions of the retina are anatomically and molecularly distinct, facilitating unique functions and demonstrating differential susceptibility to disease. Proteomic analysis of each of these regions and layers can provide vital insights into the molecular process of many diseases, including Age-Related Macular Degeneration (AMD), diabetes mellitus, and glaucoma. However, separation of retinal regions and layers is essential before quantitative proteomic analysis can be accomplished. Here, we describe a method for dissection and collection of the foveal, macular, and peripheral retinal regions and underlying RPE-choroid complex, involving regional punch biopsies and manual removal of tissue layers from a human eye.One-dimensional SDS-PAGE as well as downstream proteomic analysis, such as liquid chromatography-tandem mass spectrometry (LC-MS/MS), can be used to identify proteins in each dissected retinal layer, revealing molecular biomarkers for retinal disease.

The human retina is composed of functionally and molecularly distinct regions, including the fovea, macula, and peripheral retina. Here, we describe a method using punch biopsies and manual removal of tissue layers from a human eye to dissect and collect these distinct retinal regions for downstream proteomic analysis.

The human retina is composed of the sensory neuroretina and the underlying retinal pigmented epithelium (RPE), which is firmly complexed to the vascular ...

Biochemistry

Consensus Brain-derived Protein, Extraction Protocol for the Study of Human and Murine Brain Proteome Using Both 2D-DIGE and Mini 2DE Immunoblotting

Two-dimensional gel electrophoresis (2DE) is a powerful tool to uncover proteome modifications potentially related to different physiological or pathological conditions. Basically, this technique is based on the separation of proteins according to their isoelectric point in a first step, and secondly according to their molecular weights by SDS polyacrylamide gel electrophoresis (SDS-PAGE). In this report an optimized sample preparation protocol for little amount of human post-mortem and mouse brain tissue is described. This method enables to perform both two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) and mini 2DE immunoblotting. The combination of these approaches allows one to not only find new proteins and/or protein modifications in their expression thanks to its compatibility with mass spectrometry detection, but also a new insight into markers validation. Thus, mini-2DE coupled to western blotting permits to identify and validate post-translational modifications, proteins catabolism and provides a qualitative comparison among different conditions and/or treatments. Herein, we provide a method to study components of protein aggregates found in AD and Lewy body dementia such as the amyloid-beta peptide and the alpha-synuclein. Our method can thus be adapted for the analysis of the proteome and insoluble proteins extract from human brain tissue and mice models too. In parallel, it may provide useful information for the study of molecular and cellular pathways involved in neurodegenerative diseases as well as potential novel biomarkers and therapeutic targets.

A common protein extraction protocol using urea/thiourea/SDS buffer for human and mice brain tissue allows indentification of proteins by 2D-DIGE and their subsequent characterization by mini 2DE immunoblotting. This method enables one to obtain more reproducible and reliable results from human biopsies and experimental models.

Two-dimensional gel electrophoresis (2DE) is a powerful tool to uncover proteome modifications potentially related to different physiological or ...

Lipidomics and Transcriptomics in Neurological Diseases

Lipids serve as the primary interface to brain insults or stimuli conducive to neurological diseases and are a reservoir for the synthesis of lipids with various signaling or ligand function that can underscore the onset and progression of diseases. Often changing at the presymptomatic level, lipids are an emerging source of drug targets and biomarkers. Many neurological diseases exhibit neuroinflammation, neurodegeneration, and neuronal excitability as common hallmarks, partly modulated by specific lipid signaling systems. The interdependence and interrelation of synthesis of various lipids prompts a multilipid, multienzyme, and multireceptor analysis in order to derive the commonalities and specificities of neurological contexts and to expedite the unravelling of mechanistic aspects of disease onset and progression. Ascribing lipid roles to distinct brain regions advances the determination of lipid molecular phenotype and morphology associated with a neurological disease.
Presented here is a modular protocol suitable for the analysis of membrane lipids and downstream lipid signals along with mRNA of enzymes and mediators underlying their functionality, extracted from discrete brain regions that are relevant for a particular neurological disease and/or condition. To ensure accurate comparative lipidomic profiling, the workflows and operating criteria were optimized and standardized for: i) brain sampling and dissection of regions of interest, ii) co-extraction of multiple lipid signals and membrane lipids, iii) dual lipid/mRNA extraction, iv) quantification by liquid chromatography multiple reaction monitoring (LC/MRM), and v) standard mRNA profiling. This workflow is amenable for the low tissue amounts obtained by sampling of the functionally discrete brain subregions (i.e. by brain punching), thus preventing bias in multimolecular analysis due to tissue heterogeneity and/or animal variability. To reveal peripheral consequences of neurological diseases and establish translational molecular readouts of neurological disease states, peripheral organ sampling, processing, and their subsequent lipidomic analysis, as well as plasma lipidomics, are also pursued and described. The protocol is demonstrated on an acute epilepsy mouse model.

This article presents a modular protocol for tissue lipidomics and transcriptomics, and plasma lipidomics in neurological disease mouse models targeting lipids underlying inflammation and neuronal activity, membrane lipids, downstream messengers, and mRNA-encoding enzymes/receptors underlying lipid function. Sampling, sample processing, extraction, and quantification procedures are outlined.

Lipids serve as the primary interface to brain insults or stimuli conducive to neurological diseases and are a reservoir for the synthesis of lipids with ...

Quantifying Subcellular Ubiquitin-proteasome Activity in the Rodent Brain

The ubiquitin-proteasome system is a key regulator of protein degradation and a variety of other cellular processes in eukaryotes. In the brain, increases in ubiquitin-proteasome activity are critical for synaptic plasticity and memory formation and aberrant changes in this system are associated with a variety of neurological, neurodegenerative and psychiatric disorders. One of the issues in studying ubiquitin-proteasome functioning in the brain is that it is present in all cellular compartments, in which the protein targets, functional role and mechanisms of regulation can vary widely. As a result, the ability to directly compare brain ubiquitin protein targeting and proteasome catalytic activity in different subcellular compartments within the same animal is critical for fully understanding how the UPS contributes to synaptic plasticity, memory and disease. The method described here allows collection of nuclear, cytoplasmic and crude synaptic fractions from the same rodent (rat) brain, followed by simultaneous quantification of proteasome catalytic activity (indirectly, providing activity of the proteasome core only) and linkage-specific ubiquitin protein tagging. Thus, the method can be used to directly compare subcellular changes in ubiquitin-proteasome activity in different brain regions in the same animal during synaptic plasticity, memory formation and different disease states. This method can also be used to assess the subcellular distribution and function of other proteins within the same animal.

This protocol is designed to efficiently quantify ubiquitin-proteasome system (UPS) activity in different cellular compartments of the rodent brain. Users are able to examine UPS functioning in nuclear, cytoplasmic and synaptic fractions in the same animal, reducing the amount of time and number of animals needed to perform these complex analyses.

The ubiquitin-proteasome system is a key regulator of protein degradation and a variety of other cellular processes in eukaryotes. In the brain, increases ...

Collection of Frozen Rodent Brain Regions for Downstream Analyses

As our understanding of neurobiology has progressed, molecular analyses are often performed on small brain areas such as the medial prefrontal cortex (mPFC) or nucleus accumbens. The challenge in this work is to dissect the correct area while preserving the microenvironment to be examined. In this paper, we describe a simple, low-cost method using resources readily available in most labs. This method preserves nucleic acid and proteins by keeping the tissue frozen throughout the process. Brains are cut into 0.5&#8211;1.0 mm sections using a brain matrix and arranged on a frozen glass plate. Landmarks within each section are compared to a reference, such as the Allen Mouse Brain Atlas, and regions are dissected using a cold scalpel or biopsy punch. Tissue is then stored at -80 &#176;C until use. Through this process rat and mouse mPFC, nucleus accumbens, dorsal and ventral hippocampus and other regions have been successfully analyzed using qRT-PCR and Western assays. This method is limited to brain regions that can be identified by clear landmarks.

This procedure describes the collection of discrete frozen brain regions to obtain high-quality protein and RNA using inexpensive and commonly available tools.

As our understanding of neurobiology has progressed, molecular analyses are often performed on small brain areas such as the medial prefrontal cortex ...

Semi-Quantitative Determination of Dopaminergic Neuron Density in the Substantia Nigra of Rodent Models using Automated Image Analysis

Estimation of the number of dopaminergic neurons in the substantia nigra is a key method in pre-clinical Parkinson's disease research. Currently, unbiased stereological counting is the standard for quantification of these cells, but it remains a laborious and time-consuming process, which may not be feasible for all projects. Here, we describe the use of an image analysis platform, which can accurately estimate the quantity of labeled cells in a pre-defined region of interest. We describe a step-by-step protocol for this method of analysis in rat brain and demonstrate it can identify a significant reduction in tyrosine hydroxylase positive neurons due to expression of mutant &#945;-synuclein in the substantia nigra. We validated this methodology by comparing with results obtained by unbiased stereology. Taken together, this method provides a time-efficient and accurate process for detecting changes in dopaminergic neuron number, and thus is suitable for efficient determination of the effect of interventions on cell survival.

Here we present an automated method for semi-quantitative determination of dopaminergic neuron number in the rat substantia nigra pars compacta.

Estimation of the number of dopaminergic neurons in the substantia nigra is a key method in pre-clinical Parkinson's disease research. Currently, unbiased ...

Isolation of Adult Human Astrocyte Populations from Fresh-Frozen Cortex Using Fluorescence-Activated Nuclei Sorting

The complexity of human astrocytes remains poorly defined in primary human tissue, requiring better tools for their isolation and molecular characterization. Fluorescence-activated nuclei sorting (FANS) can be used to successfully isolate and study human neuronal nuclei (NeuN+) populations from frozen archival tissue, thereby avoiding problems associated with handling&#160;fresh tissue. However, efforts to similarly isolate astroglia from the non-neuronal (NeuN-) element are lacking. A recently developed and validated immunotagging strategy uses three transcription factor antibodies to simultaneously isolate enriched neuronal (NeuN+), astrocyte (paired box protein 6 (PAX6)+NeuN-), and oligodendrocyte progenitor (OLIG2+NeuN-) nuclei populations from non-diseased, fresh (unfixed) snap-frozen&#160;postmortem human temporal neocortex tissue.
This technique was shown to be useful for the characterization of cell type-specific transcriptome alterations in primary pathological epilepsy neocortex. Transcriptomic analyses confirmed that PAX6+NeuN- sorted populations are robustly enriched for pan-astrocyte markers and capture astrocytes in both resting and reactive conditions. This paper describes the FANS methodology for the isolation of astrocyte-enriched nuclei populations from fresh-frozen human cortex, including tissue dissociation into single-nucleus (sn) suspension; immunotagging of nuclei with anti-NeuN and anti-PAX6 fluorescently conjugated antibodies; FANS gating strategies and quality control metrics for optimizing sensitivity and specificity during sorting and for confirming astrocyte enrichment; and recommended procurement for downstream transcriptome and chromatin accessibility sequencing at bulk or sn resolution. This protocol is applicable for non-necrotic, fresh-frozen, human cortical specimens with various pathologies and recommended postmortem tissue collection within 24 h.

We have developed a method that enriches for and isolates human astrocyte populations from fresh-frozen tissue for use in downstream molecular analyses.

The complexity of human astrocytes remains poorly defined in primary human tissue, requiring better tools for their isolation and molecular ...

Microdissection and Whole Mount Scanning Electron Microscopy Visualization of Mouse Choroid Plexus

The choroid plexus (CP), a highly vascularized structure protruding into the ventricles of the brain, is one of the most understudied tissues in neuroscience. As it is becoming increasingly clear that this tiny structure plays a crucial role in health and disease of the central nervous system (CNS), it is of utmost importance to properly dissect the CP out of the brain ventricles in a way that allows downstream processing, ranging from functional to structural analysis. Here, isolation of the lateral and fourth brain ventricle mouse CP without the need for specialized tools or equipment is described. This isolation technique preserves the viability, function, and structure of cells within the CP. On account of its high vascularization, the CP can be visualized floating inside the ventricular cavities of the brain using a binocular microscope. However, transcardial perfusion required for downstream analysis can complicate the identification of the CP tissue. Depending on the further processing steps (e.g., RNA and protein analysis), this can be solved by visualizing the CP via transcardial perfusion with bromophenol blue. After isolation, the CP can be processed using several techniques, including RNA, protein, or single cell analysis, to gain further understanding on the function of this special brain structure. Here, scanning electron microscopy (SEM) on whole mount CP is used to get an overall view of the structure.

The choroid plexus (CP), an understudied tissue in neuroscience, plays a key role in health and disease of the central nervous system. This protocol describes a microdissection technique for isolating the CP and the use of scanning electron microscopy to obtain an overall view of its cellular structure.

The choroid plexus (CP), a highly vascularized structure protruding into the ventricles of the brain, is one of the most understudied tissues in ...

Cryosectioning of Contiguous Regions of a Single Mouse Skeletal Muscle for Gene Expression and Histological Analyses

With this method, consecutive cryosections are collected to enable both microscopy applications for tissue histology and enrichment of RNA for gene expression using adjacent regions from a single mouse skeletal muscle. Typically, it is challenging to achieve adequate homogenization of small skeletal muscle samples because buffer volumes may be too low for efficient grinding applications, yet without sufficient mechanical disruption, the dense tissue architecture of muscle limits penetration of buffer reagents, ultimately causing low RNA yield. By following the protocol reported here, 30 &#956;m sections are collected and pooled allowing cryosectioning and subsequent needle homogenization to mechanically disrupt the muscle, increasing the surface area exposed for buffer penetration. The primary limitations of the technique are that it requires a cryostat, and it is relatively low throughput. However, high-quality RNA can be obtained from small samples of pooled muscle cryosections, making this method accessible for many different skeletal muscles and other tissues. Furthermore, this technique enables matched analyses (e.g., tissue histopathology and gene expression) from adjacent regions of a single skeletal muscle so that measurements can be directly compared across applications to reduce experimental uncertainty and to reduce replicative animal experiments necessary to source a small tissue for multiple applications.

Consecutive cryo-sections are collected to enable histological applications and enrichment of RNA for gene expression measurements using adjacent regions from a single mouse skeletal muscle. High-quality RNA is obtained from 20 - 30 mg of pooled cryosections and measurements are directly compared across applications.

With this method, consecutive cryosections are collected to enable both microscopy applications for tissue histology and enrichment of RNA for gene ...

Biology

The CryoAPEX Method for Electron Microscopy Analysis of Membrane Protein Localization Within Ultrastructurally-Preserved Cells

Key cellular events like signal transduction and membrane trafficking rely on proper protein location within cellular compartments. Understanding precise subcellular localization of proteins is thus important for answering many biological questions. The quest for a robust label to identify protein localization combined with adequate cellular preservation and staining has been historically challenging. Recent advances in electron microscopy (EM) imaging have led to the development of many methods and strategies to increase cellular preservation and label target proteins. A relatively new peroxidase-based genetic tag, APEX2, is a promising leader in cloneable EM-active tags. Sample preparation for transmission electron microscopy (TEM) has also advanced in recent years with the advent of cryofixation by high pressure freezing (HPF) and low-temperature dehydration and staining via freeze substitution (FS). HPF and FS provide excellent preservation of cellular ultrastructure for TEM imaging, second only to direct cryo-imaging of vitreous samples. Here we present a protocol for the cryoAPEX method, which combines the use of the APEX2 tag with HPF and FS. In this protocol, a protein of interest is tagged with APEX2, followed by chemical fixation and the peroxidase reaction. In place of traditional staining and alcohol dehydration at room temperature, the sample is cryofixed and undergoes dehydration and staining at low temperature via FS. Using cryoAPEX, not only can a protein of interest be identified within subcellular compartments, but also additional information can be resolved with respect to its topology within a structurally preserved membrane. We show that this method can provide high enough resolution to decipher protein distribution patterns within an organelle lumen, and to distinguish the compartmentalization of a protein within one organelle in close proximity to other unlabeled organelles. Further, cryoAPEX is procedurally straightforward and amenable to cells grown in tissue culture. It is no more technically challenging than typical cryofixation and freeze substitution methods. CryoAPEX is widely applicable for TEM analysis of any membrane protein that can be genetically tagged.

This protocol describes the cryoAPEX method, in which an APEX2-tagged membrane protein can be localized by transmission electron microscopy within optimally-preserved cell ultrastructure.

Key cellular events like signal transduction and membrane trafficking rely on proper protein location within cellular compartments. Understanding precise ...

Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis

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