这项研究是由德意志研究联合会GraKo1121，Hu1011/2-1和SFB940到上海的资金支持

注: 表1是关于可在协议中表示缓冲区的详细信息。 1。蛋白质 - 蛋白质相互作用的甲醛交联的活细胞固定<ol><li>要开始准备的生长介质，原液和缓冲P1 <ol><li>制备500mL介质:该介质应该提供支持膜诱饵蛋白和猎物蛋白之间的相互作用的条件。此外，一个实验应该在没有相互作用，预期（ 例如，未经交联）的条件下进行。 注意:我们比较蛋白质 - 蛋白质相互作用中强调和非强调的细菌。因此，我们制备500mL的Luria BERTANI（LB）培养基中（ 表1），我们有应激诱导剂（ 例如，0.5M氯化钠）中的2升锥形烧瓶中补充。为控制中，我们使用正常的LB培养基中以0.17 M氯化钠（pH 7.0）中。 </li><li>制备的Tris-缓冲液（20mM的Tris-H氯，pH值8.0）和0.1M乙二胺四乙酸（EDTA），pH值8.0储备溶液（ 表1）。 </li><li>准备缓冲区P1。蔗糖溶解到0.5M的在Tris-缓冲液中的最终浓度。消毒缓冲P1通过过滤，并将其存储在4℃下</li></ol></li><li>生长细胞中表达的膜蛋白诱饵与从向量的C-末端Strep-标签融合。诱导膜诱饵蛋白进行足够时间的表达。 注意:我们通过加入250μl的1M的异丙基-β-D-硫代半乳糖苷（IPTG）至500ml培养基中诱导细菌膜诱饵蛋白的表达在早期的对数期（A 600 = 0.3）（终浓度为0.5mM） 。为预留足够的表达，我们培养细菌，直到后期日志相（A 600 = 1.2）。 </li><li>每个文化中两种离心机烧杯准备与各300ml最小体积，并把它们放在冰上。 </li><li>执行甲醛交联。 中国农业大学TION:甲醛是剧毒的建议下，安全通风柜工作。 <ol><li>转下安全通风柜培养容器。每个样品分成两个样品，1省略了交联（ - X）和1包括交联的甲醛（X +）。加4毫升37％甲醛溶液至250毫升培养物达到0.6％的终浓度。 </li></ol></li><li>转让培养容器回来，像以前一样培养细胞进行进一步20分钟。 </li><li>请填写你的文化变成下一个安全通风柜的离心管。离心3000×g离心30分钟收集细胞。 </li><li>通过在一个安全的通风柜仔细吹打起来弃上清液。收集有毒含甲醛上清液并妥善处置。 </li><li>为了膜蛋白制备过程中达到最佳的产量，先准备原生质球。这里，我们提供了一个协议，用于原生质球形成的革兰氏阴性菌: <ol><li> PreparË缓冲P2（ 表1）从冻干粉。轻轻地溶解2毫克溶菌酶在0.1M EDTA，pH为8，在1.5ml管中。总是新鲜制备缓冲液P2为在实验的当天。 </li><li>制备的Tris-缓冲液中的蛋白酶抑制剂（缓冲液P3）。到10毫升的Tris-缓冲液中，加入0.1毫升的1摩尔苯甲基磺酰氟（PMSF）（ 表1），以10mM的终浓度。立即使用缓冲区，以确保PMSF的正常功能作为蛋白酶抑制剂。 </li><li>重悬细胞沉淀物在10毫升的Tris-缓冲液中蛋白酶抑制剂和转移溶液到15毫升锥形管中。 </li><li>加入1 ml缓冲液P2，并在冰上孵育30分钟。 </li><li>经离心收集原生质球在3000×g离心30分钟，小心弃去上清液。 </li></ol></li><li>过夜孵育原生质球丸粒在-20℃下</li></ol> 2。的Strep-标签膜蛋白的纯化（诱饵） <ol><li>将原生质体沉淀置于冰上。&lt;/ LI&gt; <li>在当时的球状体颗粒融化冰，准备好10 ml缓冲液P3每个原生质体的制备。轻轻地溶解1毫克DNA酶I在10毫升的Tris-缓冲液中。加入0.1毫升的1摩尔PMSF使用前。 </li><li>重悬沉淀6毫升新鲜配制P3。超声处理的样品4次，用于连续1分钟在冰上用每个脉冲串之间的1分钟的停顿，以破坏球状体。 </li><li>离心样品以10,000 xg离心10分钟以收获细胞碎片。用移液管向一个超速离心管转移上清液。 </li><li>沉淀膜级分以100,000×g离心30分钟。不溶解于Tris缓冲仔细洗涤沉淀。干管与纸巾（ 如纸巾）。避免打扰沉淀在任何时候。 </li><li> 1毫升的Tris缓冲仔细悬浮颗粒（=膜）。使用20微升等分试样由例如 BCA测定来确定蛋白质浓度。在该步骤中，膜可快速冷冻在利嚼食氮气并储存于-80℃。 </li></ol> 3。的Strep-标签膜诱饵蛋白和SDS-PAGE分离纯化<ol><li>归一化膜部分的蛋白浓度为5毫克/毫升，用Tris-缓冲液中。采取2.5毫升膜部分（5毫克/毫升）在超速离心管中，加入0.25的20％的Triton X-100毫升达到2％的终浓度，以溶解的膜蛋白。加一个微磁性棒搅拌，冰浴1小时。 注:虽然一般我们在使用的Triton X-100作为洗涤剂了良好的效果，它可能是有用的改变洗涤剂进行优化。在这方面，我们已与用于各个膜诱饵蛋白的功能性纯化的那些洗涤剂最好的结果。 </li><li>而执行步骤3.1，准备50毫升从（ 表1）缓冲W和5毫升指令E。填写10毫升5X缓冲W浓缩至50毫升加入150μl20％的Triton X-100。 <ol><li>填写1毫升5倍buffeR E浓缩至10ml，加入30微升20％的Triton X-100。平衡用8ml缓冲器W的1毫升链霉素-Tactin超流重力流柱 注意:这是必要添加用于增溶的浓度10倍以上的临界胶束浓度（cmc）的任何缓冲的纯化过程中的洗涤剂。 </li></ol></li><li>从溶解样品和超速离心除去微磁性棒以100,000×g离心30分钟，以沉淀不溶性膜级分。用移液管进行进一步的纯化除去上清液。 </li><li>加载上清上柱。只与重力流运行列。用5毫升的缓冲W.洗柱重复此洗涤步骤5倍。 </li><li>洗脱膜诱饵蛋白1毫升缓冲液E.重复此洗脱步骤4倍。 </li><li>浓缩洗脱馏分2，3，和4到300微升用离心过滤单元。 </li><li>混合200μl的各样品与50μl的5×SDS-PAGê样染料。在125微升等份分割每个准备。熬每个准备20分钟的一个等分在95℃，以扭转甲醛交联。让样品冷却至室温的台式至少10分钟。 </li><li>负载从每个样品30μl到聚丙烯酰胺凝胶适合免疫的单一车道。使用预染色分子量标记为最佳方位和运行的SDS-PAGE 10。 </li></ol> 4。免疫印迹分析，以确认合作伙伴的互动<ol><li>一旦步骤3.8完成后，转移蛋白至硝酸纤维素膜，例如由半干法。 </li><li>阻断膜，以防止非特异性标记。制备封闭缓冲液通过称量牛血清白蛋白（BSA），以实现每单位体积的3％重量在Tris缓冲盐水补充有0.05％吐温20（TBS-T）的最终浓度。用封闭缓冲液以覆盖膜的足够体积。阻挡膜1小时，在室温下。 </li><li>一个稀ND孵化猎物蛋白特异性第一抗体如常。使用HRP-连接的抗体作为第二抗体。 </li><li>采用化学发光检测试剂盒具有灵敏度高发展免疫。采用经典的胶片处理过程或数码影像设备监控信号。 </li></ol> 5。 NanoLC-ESI-MS/MS高分辨率实验，以确定合作伙伴的互动<ol><li>的情况下，没有特定的抗体可用于猎物蛋白或未知的相互作用伙伴应查明，使用质谱法（MS）进行鉴定。为了防止角蛋白污染，用预制凝胶用于蛋白质的分离。 </li><li>用MS-兼容染色试剂盒根据制造商的方案银染色的SDS-PAGE。执行中玻璃坦克所有的染色和洗涤步骤。 </li><li>消费各个频段和高解析度的LC / MS 9分析这些。 </li></ol>

<ol>
	<li>Krogh, A., Larsson, B., von Heijne, G., Sonnhammer, E. L. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Predicting+transmembrane+protein+topology+with+a+hidden+markov+model:+application+to+complete+genomes.">Predicting transmembrane protein topology with a hidden markov model: application to complete genomes.</a> J. Mol. Biol. 305, 567-580 (2001).</li><li>Bakheet, T. M., Doig, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Properties+and+identification+of+human+protein+drug+targets.">Properties and identification of human protein drug targets.</a> Bioinformatics. 25, 451-457 (2009).</li><li>Yildirim, M. A., Goh, K. I., Cusick, M. E., Barabasi, A. L., Vidal, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Drug-target+network.">Drug-target network.</a> Nat. Biotechnol. 25, (2007).</li><li>Daley, D. O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+assembly+of+membrane+proteins+into+complexes.">The assembly of membrane proteins into complexes.</a> Curr. Opin. Struct. Biol. 18, 420-424 (2008).</li><li>Jung, K., Fried, L., Behr, S., Heermann, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Histidine+kinases+and+response+regulators+in+networks.">Histidine kinases and response regulators in networks.</a> Curr. Opin. Microbiol. 15, 118-124 (2012).</li><li>M&#252;ller, V. S., Jungblut, P. R., Meyer, T. F., Hunke, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Membrane-SPINE:+An+improved+method+to+identify+protein-protein+interaction+partners+of+membrane+proteins+in+vivo.">Membrane-SPINE: An improved method to identify protein-protein interaction partners of membrane proteins in vivo.</a> Proteomics. 11, 2124-2128 (2011).</li><li>Herzberg, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=SPINE:+A+method+for+the+rapid+detection+and+analysis+of+protein-protein+interactions+in+vivo.">SPINE: A method for the rapid detection and analysis of protein-protein interactions in vivo.</a> Proteomics. 7, 4032-4035 (2007).</li><li>Sutherland, B. W., Toews, J., Kast, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Utility+of+formaldehyde+cross-linking+and+mass+spectrometry+in+the+study+of+protein-protein+interactions.">Utility of formaldehyde cross-linking and mass spectrometry in the study of protein-protein interactions.</a> J. Mass Spectrom. 43, 699-715 (2008).</li><li>Hernandez, P., M&#252;ller, M., Appel, R. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Automated+protein+identification+by+tandem+mass+spectrometry:+Issues+and+strategies.">Automated protein identification by tandem mass spectrometry: Issues and strategies.</a> Mass Spectrom. Rev. 25, 235-254 (2006).</li><li>Laemmli, U. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cleavage+of+structural+proteins+during+the+assembly+of+the+head+of+bacteriophage+T4.">Cleavage of structural proteins during the assembly of the head of bacteriophage T4.</a> Nature. 227, 680-685 (1970).</li><li>Hunke, S., Keller, R., M&#252;ller, V. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Signal+integration+by+the+Cpx-envelope+stress+system.">Signal integration by the Cpx-envelope stress system.</a> FEMS Microbiol. Lett. 326, 12-22 (2012).</li><li>Weber, R. F., Silverman, P. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Cpx+proteins+of+Escherichia+coli+K12+:+Structure+of+the+CpxA+polypeptide+as+an+inner+membrane+component.">The Cpx proteins of Escherichia coli K12 : Structure of the CpxA polypeptide as an inner membrane component.</a> J. Mol. Biol. 203, 467-478 (1988).</li></ol>

我们什么都没有透露。

膜脊柱的分析是生化的方法，使一个确认，并确定膜蛋白的这点未知的互动合作伙伴。膜脊柱由甲醛与链球菌标签膜诱饵蛋白的纯化结合在体内的交联。用免疫印迹法的组合有利于预测的相互作用伙伴的确认（ 图2）。此外，与MS分析的组合允许未知的相互作用伙伴的标识（ 图3）。对于这两种应用程序，有修改你的猎物蛋白质没有要求。此外，膜脊柱是足够的敏感，使内源性蛋白质的猎物6的检测。 这里，我们提出了对革兰氏阴性菌膜蛋白而优化的协议。革兰氏阴性菌的信封从环境和posses分离细胞质，除了胞质膜，外膜和胞壁质球囊。因此，我们的协议包括除去外膜和胞壁质球囊，导致所谓的原生质球。因为这样的协议是可用于大多数类型的细胞，我们的协议应该适应于大多数膜蛋白。此外，以下几点应予以考虑。 首先，载体的拷贝数用过量的膜诱饵蛋白具有较高的电平之间进行平衡，以便有足够的膜蛋白的纯化和一个低电平，以防止非特异性相互作用第二，对于某些膜蛋白的N-末端融合可能比一个C-末端融合更优化。在这两种情况下，融合的功能应该由反式互补的确认。 第三，其它亲和纯化方案也与随后的MS分析相容的，如FLAG纯化和串联亲和纯化（TAP）。我们更喜欢，因为它只有8个氨基酸（WSHPQFEK）小尺寸的Strep-标签II。 第四，用甲醛和交联时间的浓度应进行优化，以防止非特异性交联。足够，但不能过量使用甲醛可通过未煮沸样品的免疫印迹如交联和无链接膜诱饵蛋白（ 图2）之间的比率进行监测。交联的蛋白质迁移如在免疫印迹的上部涂片。未连接的蛋白质迁移作为未处理的蛋白质。交联和未链接的蛋白质之间的比率应为约3:1。 第五，没有"一般的清洁剂"的所有膜蛋白的溶解。因此，在某些情况下，适当的洗涤剂对膜诱饵蛋白的增溶作用已被确定。从而，所选择的洗涤剂必须与Strep-标签栏的兼容Ñ​​。 最后，将银染色过程必须与随后的MS分析相容。 MS兼容的银染试剂盒可从不同的供应商。我们使用不同的人相媲美的好成绩。

了解蛋白质的功能，必须知道它的相互作用伙伴。几种传统的技术可用于可溶性蛋白的相互作用伙伴的标识。然而，这些技术是不容易转移到膜，由于其疏水性，4种蛋白。为了克服这个限制，我们已经开发了膜链球菌蛋白质相互作用实验（膜脊柱）6。它是根据脊柱的方法，它是唯一适合的可溶性蛋白7。 从两个优点的交联剂甲醛的膜-脊柱的好处:第一，甲醛可以轻易穿透细胞膜，因此产生一个活细胞8的相互作用组的精确快照。二，甲醛交联可煮沸9逆转。在这里，这两个优势是用来识别不仅永久性的，但也是短暂的膜保护制服的生产者价格指数插件6。 简言之，Strep-标签融合到完整的膜诱饵蛋白的C-末端。细胞中表达的膜蛋白诱饵孵育与甲醛的交联猎物蛋白质与膜诱饵蛋白（ 图1）。不需要猎物蛋白的修饰。接着，将膜部分准备。因此，膜蛋白是由洗涤剂处理和饵料蛋白质共同纯化，用亲和纯化它的猎物的蛋白质溶解。接着，将交联是通过煮沸颠倒，诱饵和其共洗脱猎物蛋白通过SDS-PAGE分离。最后，猎物的蛋白质可通过免疫印迹分析或质谱来识别。

<table border="0" cellpadding="0" cellspacing="0" width="878">
	<colgroup>
		<col />
		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">37% Formaldehyde</td>
			<td style="width:128px;">Roth</td>
			<td style="width:137px;">4979.1</td>
			<td style="width:271px;">Should not be older than one year</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">DNaseI</td>
			<td style="width:128px;">Sigma</td>
			<td style="width:137px;">DN25</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">BCA protein assay kit</td>
			<td style="width:128px;">Pierce</td>
			<td style="width:137px;">23225</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">Micromagnetic rod</td>
			<td style="width:128px;">Roth</td>
			<td style="width:137px;">0955.2</td>
			<td style="width:271px;">5 mm in length, 2 mm in diameter</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">Triton X-100</td>
			<td style="width:128px;">Roth</td>
			<td style="width:137px;">6683.1</td>
			<td style="width:271px;">standard detergent for solubilization</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">n-Dodecyl-&#946;-maltoside</td>
			<td style="width:128px;">Glycon</td>
			<td style="width:137px;">D97002-C</td>
			<td style="width:271px;">the best detergent to solubilze CpxA</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">1 ml Strep-Tactin superflow gravity flow column</td>
			<td style="width:128px;">IBA</td>
			<td style="width:137px;">2-1207-050</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">Strep-tag protein purification buffer set</td>
			<td style="width:128px;">IBA</td>
			<td style="width:137px;">2-1002-001</td>
			<td style="width:271px;">Contains buffer W and buffer E</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">Amicon Ultra-4 centrifugal filter</td>
			<td style="width:128px;">Millipore</td>
			<td style="width:137px;">UFC803024</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:343px;">SuperSignal West Pico Chemiluminescent substrate</td>
			<td style="width:128px;">Pierce</td>
			<td style="width:137px;">34080</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">SilverQuest Silverstaining kit</td>
			<td style="width:128px;">Invitrogen</td>
			<td style="width:137px;">LC6070</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">FireSilver Staining Kit</td>
			<td style="width:128px;">Proteome Factory</td>
			<td style="width:137px;">P-S-2001</td>
			<td style="width:271px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:343px;">Ultracentrifuge</td>
			<td style="width:128px;"></td>
			<td style="width:137px;"></td>
			<td style="width:271px;"></td>
		</tr>
	</tbody>
</table>

membrane-spine: a biochemical tool to identify protein-protein interactions of membrane proteins in vivo

膜蛋白是细胞存活必不可少的，因此是重要的治疗靶标1-3。由于他们在配合4个功能，方法来识别和描述它们之间的相互作用是必要的5。为此，我们开发了膜链球菌-蛋白相互作用的实验，称为膜脊柱6。该技术结合在体内使用可逆的交联剂甲醛与链球菌标签膜诱饵蛋白的亲和纯化的交联。在实验过程中，交联的猎物蛋白质是共纯化，用该膜诱饵蛋白，并随后通过煮沸分离。因此，两大任务可以分析蛋白质 - 蛋白质相互作用的膜蛋白（生产者价格指数），当使用膜脊柱执行:首先，提出一个合作伙伴的交互通过免疫印迹，并确认第二，新的互动合作伙伴通过质谱分析鉴定。而且，即使升嗷嗷的亲和力，瞬间PPIs是检测用这种技术。最后，膜脊柱是适用于几乎任何类型的细胞，使其适用于作为一个强大的筛选工具，以确定膜蛋白的生产者价格指数。

膜脊柱分析可以共同净化膜蛋白和瞬时相互作用蛋白的合作伙伴。共纯化是通过使用交联剂的甲醛来实现。两个参数是关键的，以防止非特异性交联:甲醛的浓度和交联时间。足够的，但不能过量使用甲醛可以很容易地通过免疫印迹法进行控制。甲醛交联的蛋白质复合物可以通过煮沸而不是由SDS处理进行分离。因此，它们可以在链球菌二型标签膜诱饵蛋白印迹如涂抹在免疫印迹的未煮沸样品的上半部分后进行可视化。 膜脊柱检测，包括所有必需的控制具有代表性的结果，是在图2。作为诱饵蛋白大肠杆菌的整合膜蛋白CpxA使用6,11。 CpxA是传感器激酶，由一个N-末端结构域的传感器具有两个跨膜结构域（TMD）的结合的大细胞质外传感器结构域和C-末端的高度保守的胞质催化结构域12。刺激后，CpxA激活其同源反应调节CPXR。激活CPXR扩散关闭调解的响应。对于膜脊柱，使Strep-标签融合到CpxA（CpxA-链球菌）的C-末端。 CpxA -链霉素交联到被检测作为生水甲醛处理过的样品中的涂抹标本（ 图2，第1行与第3行），指出充分交联的其它蛋白质或蛋白质复合物。此外，CpxA-链球菌的与其同源响应调节蛋白CPXR作为猎物蛋白的直接蛋白质-蛋白质相互作用是在甲醛存在下只检测到（ 图2，第2行与第4行）支承甲醛交联的特异性。 膜脊柱的分析具有代表性的结果，提出我n 图3。相应于图2中的样品是银染色。箭头标记带，其特异于煮沸样品。由于背景下，MS分析还发现其他蛋白质除了CPXR 6。因此，非甲醛处理过的样品要经常进行分析，以分配背景噪声和特异性相互作用伙伴。 表1:所需的膜脊柱缓冲液和试剂。 <table border="1"><tbody><tr><th>缓冲器/试剂/中</th><th>工作浓度</th><th>评论</th></tr><tr><td> LB </td><td> 10g胰蛋白胨 5g酵母提取物 10克氯化钠至1L， 调节pH值至7.0 </td><td></td><td>卢里亚肉汤培养基</td></tr><tr><td> IPTG </td><td> 1M的异丙基-β-D-硫代半乳糖苷</td><td> 0.5毫米</td><td></td></tr><tr><td> 的Tris-缓冲</td><td>的20mM的Tris-HCl，pH值8 </td><td></td><td>用NaOH调节pH值至8.0 </td></tr><tr><td> 0.1M的EDTA，pH为8 </td><td> 0.1M的EDTA </td><td></td><td>用NaOH调节pH值至8.0 </td></tr><tr><td> PMSF </td><td> 1M的苯甲在100％异丙醇</td><td> 10毫米</td><td> PMSF稳定在100％异丙醇，不溶于水！原液可以贮存于-20℃; PMSF必须适应于室温下稀释在缓冲之前，应在制备的10分钟用在含有缓冲液的PMSF。 </td></tr><tr><td> P1 </td><td>的20mM的Tris-HCl，pH 8.0的 0.5M的蔗糖</td><td></td><td></td></tr><tr><td> P2 </td><td> 2毫克/毫升的溶菌酶在0.1 M EDTA，pH为7.5 </td><td></td><td></td></tr><tr><td> P3 </td><td>的20mM的Tris-HCl，pH 8.0的 10 mM的PMSF </td><td></td><td>使用immediately后准备</td></tr><tr><td> 洗涤剂 </td><td> 20％的Triton X-100 </td><td>增溶2％ </td><td></td></tr><tr><td> 缓冲W </td><td>填写10毫升5倍浓缩至50ml 加入150μl20％的Triton X-100 </td><td>的100mM的Tris-HCl，pH 8.0的 150 mM氯化钠 1mM EDTA的0.06％的Triton X-100 </td><td> 5倍浓缩液是Strep-标签蛋白纯化缓冲液组（IBA）的一部分</td></tr><tr><td> 缓冲液E </td><td>填写1毫升5倍浓缩至10 ml 加入30微升20％的Triton X-100 </td><td>的100mM的Tris-HCl，pH 8.0的 150 mM氯化钠 1毫米EDTA 2.5mM的脱硫生物素0.06％的Triton X-100 </td><td> 5倍浓缩液是Strep-标签蛋白纯化缓冲液组（IBA）的一部分</td></tr><tr><td> 5×SDS-PAGE上样染料 </td><td> 0.3125摩尔Tris-盐酸，pH为6.8 10％SDS 0.5 M DTT 50％甘油<br/&gt; 0.05％溴酚蓝</td><td></td><td></td></tr></tbody></table><img alt="图1" fo:content-width="6in" src="/files/ftp_upload/50810/50810fig1.jpg" width="500px" /> 图1。利用大肠杆菌膜蛋白作为诱饵蛋白A）细菌表达链球菌标签膜诱饵蛋白与甲醛处理流程图的膜脊柱过程 。甲醛渗透膜和交联捕食蛋白与膜诱饵蛋白B）的膜部分的制备和膜蛋白通过去污剂处理溶解。随后，猎物蛋白质是共纯化，用诱饵蛋白C）的甲醛的交联是由沸腾逆转和蛋白质通过SDS-PAGE分离。最后，猎物的蛋白质或者通过免疫印迹法（D）或监测确定的MS-ANA裂解（E） <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/50810/50810fig1highres.jpg" target="_blank">点击此处查看大图</a> 。 <img alt="图2" fo:content-width="6in" src="/files/ftp_upload/50810/50810fig2.jpg" width="500px" /> 图2。用于监测膜蛋白的PPI代表性免疫印迹。细菌的质粒作为膜诱饵蛋白生产CpxA -链霉素，生长在LB培养基中至OD 600为1，并暴露于甲醛（CH 2 O）20分钟。内层膜级分的制备，膜蛋白通过去污剂处理溶解和CpxA - 链霉素纯化（泳道1和2）。细菌产生不CpxA-链球菌无甲醛处理（泳道3和4）或携带空载体用甲醛处理（泳道5,5）作为对照组。每个样品的等分试样煮沸，在95℃20分钟（泳道2,4和6），以从CpxA-链球菌分离交联的蛋白质。蛋白分离以12.5％SDS-PAGE。免疫印迹按照CpxA - 链霉素（51 kDa）的大小和相应的猎物蛋白CPXR（26 kDa）的执行，并且印迹分离。 ，免疫印迹的两个部分中孵育与针对CpxA和CPXR多克隆抗体分别。随后，将印迹进一步用抗兔马（HRP）抗体和使用的SuperSignal西皮克化学发光底物研制。箭头标志CpxA的降解产物。 <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/50810/50810fig2highres.jpg" target="_blank">点击这里查看大图</a> 。 <img alt="图3" fo:content-width="6in" src="/files/ftp_upload/50810/50810fig3.jpg" width="500px" /> 图3。用于一个i的标识代表银染色的SDS-PAGE的膜蛋白的质谱分析nteraction伙伴。相应于图2中的样品银染色。该箭头标记这是由质谱分析法分析并确认CPXR作为CpxA 5的互动合作伙伴带。巷7所示纯化CPXR，他的6车道和8显示纯化CpxA，他的6蛋白。 <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/50810/50810fig3highres.jpg" target="_blank">点击这里查看大图</a> 。

Watch this Scientific Journal Video about Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo at JoVE.com

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

一个生化方法描述识别体内蛋白质膜蛋白的相互作用（PPI）。该方法结合了蛋白质的交联，亲和纯化和质谱法，并且是适合于几乎任何类型的细胞或生物体。用这种方法，瞬态质子泵抑制剂的甚至识别成为可能。

膜脊柱:一个生化工具来确定膜蛋白的蛋白质 - 蛋白质相互作用<em&gt;在体内</em

Membrane proteins are essential for cell viability and are therefore important therapeutic targets1-3. Since they function in complexes4, methods to ...

membrane-spine-biochemical-tool-to-identify-protein-protein

Nanyang Technological University

Research

JoVE Journal

Bioengineering

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

13.7K 次观看.  Universität Osnabrück. 一个生化方法描述识别体内蛋白质膜蛋白的相互作用（PPI）。该方法结合了蛋白质的交联，亲和纯化和质谱法，并且是适合于几乎任何类型的细胞或生物体。用这种方法，瞬态质子泵抑制剂的甚至识别成为可能。 

视频: Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

Fabrication of Electrochemical-DNA Biosensors for the Reagentless Detection of Nucleic Acids, Proteins and Small Molecules

As medicine is currently practiced, doctors send specimens to a central laboratory for testing and thus must wait hours or days to 
receive the results. Many patients would be better served by rapid, bedside tests. To this end our laboratory and others have developed a versatile, reagentless 
biosensor platform that supports the quantitative, reagentless, electrochemical detection of nucleic acids (DNA, RNA), proteins (including antibodies) and small 
molecules analytes directly in unprocessed clinical and environmental samples. In this video, we demonstrate the preparation and use of several biosensors in this 
"E-DNA" class. In particular, we fabricate and demonstrate sensors for the detection of a target DNA sequence in a polymerase chain reaction mixture, an HIV-specific antibody and the drug cocaine. The preparation procedure requires only three hours of hands-on effort followed by an overnight incubation, and their use requires only minutes.

"E-DNA" sensors, reagentless, electrochemical biosensors that perform well even when challenged directly in blood and other complex matrices, have been adapted to the detection of a wide range of nucleic acid, protein and small molecule analytes. Here we present a general procedure for the fabrication and use of such sensors.

无试剂检测核酸，蛋白质和小分子的电化学DNA生物传感器的制备

As medicine is currently practiced, doctors send specimens to a central laboratory for testing and thus must wait hours or days to 
receive the results. ...

科研

生物工程

Design of a Cyclic Pressure Bioreactor for the Ex Vivo Study of Aortic Heart Valves

The aortic valve, located between the left ventricle and the aorta, allows for unidirectional blood flow, preventing backflow into the ventricle. Aortic valve leaflets are composed of interstitial cells suspended within an extracellular matrix (ECM) and are lined with an endothelial cell monolayer. The valve withstands a harsh, dynamic environment and is constantly exposed to shear, flexion, tension, and compression. Research has shown calcific lesions in diseased valves occur in areas of high mechanical stress as a result of endothelial disruption or interstitial matrix damage1-3. Hence, it is not surprising that epidemiological studies have shown high blood pressure to be a leading risk factor in the onset of aortic valve disease4. 
The only treatment option currently available for valve disease is surgical replacement of the diseased valve with a bioprosthetic or mechanical valve5. Improved understanding of valve biology in response to physical stresses would help elucidate the mechanisms of valve pathogenesis. In turn, this could help in the development of non-invasive therapies such as pharmaceutical intervention or prevention. Several bioreactors have been previously developed to study the mechanobiology of native or engineered heart valves6-9. Pulsatile bioreactors have also been developed to study a range of tissues including cartilage10, bone11 and bladder12. The aim of this work was to develop a cyclic pressure system that could be used to elucidate the biological response of aortic valve leaflets to increased pressure loads. 
The system consisted of an acrylic chamber in which to place samples and produce cyclic pressure, viton diaphragm solenoid valves to control the timing of the pressure cycle, and a computer to control electrical devices. The pressure was monitored using a pressure transducer, and the signal was conditioned using a load cell conditioner. A LabVIEW program regulated the pressure using an analog device to pump compressed air into the system at the appropriate rate. The system mimicked the dynamic transvalvular pressure levels associated with the aortic valve; a saw tooth wave produced a gradual increase in pressure, typical of the transvalvular pressure gradient that is present across the valve during diastole, followed by a sharp pressure drop depicting valve opening in systole. The LabVIEW program allowed users to control the magnitude and frequency of cyclic pressure. The system was able to subject tissue samples to physiological and pathological pressure conditions. This device can be used to increase our understanding of how heart valves respond to changes in the local mechanical environment.

Design of a Cyclic Pressure Bioreactor for the Ex Vivo Study of Aortic Heart Valves

A cyclic pressure bioreactor capable of subjecting heart valve tissue to physiological and pathological pressure conditions has been designed. A LabVIEW program allows users to control pressure magnitude, amplitude and frequency. This device can be used to study the mechanobiology of heart valve tissue or isolated cells.

循环压力为生物反应器的设计体外主动脉心脏瓣膜的研究

The aortic valve, located between the left ventricle and the aorta, allows for unidirectional blood flow, preventing backflow into the ventricle. Aortic ...

Determination of the Transport Rate of Xenobiotics and Nanomaterials Across the Placenta using the ex vivo Human Placental Perfusion Model

Decades ago the human placenta was thought to be an impenetrable barrier between mother and unborn child. However, the discovery of thalidomide-induced birth defects and many later studies afterwards proved the opposite. Today several harmful xenobiotics like nicotine, heroin, methadone or drugs as well as environmental pollutants were described to overcome this barrier. With the growing use of nanotechnology, the placenta is likely to come into contact with novel nanoparticles either accidentally through exposure or intentionally in the case of potential nanomedical applications. Data from animal experiments cannot be extrapolated to humans because the placenta is the most species-specific mammalian organ 1. Therefore, the ex vivo dual recirculating human placental perfusion, developed by Panigel et al. in 1967 2 and continuously modified by Schneider et al. in 1972 3, can serve as an excellent model to study the transfer of xenobiotics or particles.
Here, we focus on the ex vivo dual recirculating human placental perfusion protocol and its further development to acquire reproducible results.
The placentae were obtained after informed consent of the mothers from uncomplicated term pregnancies undergoing caesarean delivery. The fetal and maternal vessels of an intact cotyledon were cannulated and perfused at least for five hours. As a model particle fluorescently labelled polystyrene particles with sizes of 80 and 500 nm in diameter were added to the maternal circuit. The 80 nm particles were able to cross the placental barrier and provide a perfect example for a substance which is transferred across the placenta to the fetus while the 500 nm particles were retained in the placental tissue or maternal circuit. The ex vivo human placental perfusion model is one of few models providing reliable information about the transport behavior of xenobiotics at an important tissue barrier which delivers predictive and clinical relevant data.

Determination of the Transport Rate of Xenobiotics and Nanomaterials Across the Placenta using the ex vivo Human Placental Perfusion Model

The ex vivo dual recirculating human placental perfusion model can be used to investigate the transfer of xenobiotics and nanoparticles across the human placenta. In this video protocol we describe the equipment and techniques required for a successful execution of a placenta perfusion.

通过胎盘的外来物质和纳米材料的运输率测定<em&gt;体外</em&gt;人胎盘灌注型号

Decades ago the human placenta was thought to be an impenetrable barrier between mother and unborn child. However, the discovery of thalidomide-induced ...

Isolation and Characterization Of Chimeric Human Fc-expressing Proteins Using Protein A Membrane Adsorbers And A Streamlined Workflow

Laboratory scale to industrial scale purification of biomolecules from cell culture supernatants and lysed cell solutions can be accomplished using affinity chromatography.&#160;While affinity chromatography using porous protein A agarose beads packed in columns is arguably the most common method of laboratory scale isolation of antibodies and recombinant proteins expressing Fc fragments of IgG, it can be a time consuming and expensive process.&#160;Time and financial constraints are especially daunting in small basic science labs that must recover hundreds of micrograms to milligram quantities of protein from dilute solutions, yet lack access to high pressure liquid delivery systems and/or personnel with expertise in bioseparations. Moreover, product quantification and characterization may also excessively lengthen processing time over several workdays and inflate expenses (consumables, wages, etc.).&#160;Therefore, a fast, inexpensive, yet effective protocol is needed for laboratory scale isolation and characterization of antibodies and other proteins possessing an Fc fragment.&#160;To this end, we have devised a protocol that can be completed by limited-experience technical staff in less than 9 hr (roughly one workday) and as quickly as 4 hr, as opposed to traditional methods that demand 20+ work hours. Most required equipment is readily available in standard biomedical science, biochemistry, and (bio)chemical engineering labs, and all reagents are commercially available.&#160;To demonstrate this protocol, representative results are presented in which chimeric&#160;murine galectin-1 fused to human Fc (Gal-1hFc) from cell culture supernatant was isolated using a protein A membrane adsorber.&#160;Purified Gal-1hFc was quantified using an expedited Western blotting analysis procedure and characterized using flow cytometry. The streamlined workflow can be modified for other Fc-expressing proteins, such as antibodies, and/or altered to incorporate alternative quantification and characterization methods.

Compared with traditional affinity chromatography using protein A agarose bead-packed columns, protein A membrane adsorbers can significantly speed laboratory-scale isolation of antibodies and other Fc fragment-expressing proteins.&#160;Appropriate analysis and quantification methods can further accelerate protein processing, allowing isolation/characterization to be completed in one workday, instead of 20+ work hours.

使用蛋白质膜吸收器和流线型工作流的奇美人 Fc 表达蛋白质的隔离和特征

Laboratory scale to industrial scale purification of biomolecules from cell culture supernatants and lysed cell solutions can be accomplished using ...

Luminescence Resonance Energy Transfer to Study Conformational Changes in Membrane Proteins Expressed in Mammalian Cells

Luminescence Resonance Energy Transfer, or LRET, is a powerful technique used to measure distances between two sites in proteins within the distance range of 10-100 &#197;. By measuring the distances under various ligated conditions, conformational changes of the protein can be easily assessed. With LRET, a lanthanide, most often chelated terbium, is used as the donor fluorophore, affording advantages such as a longer donor-only emission lifetime, the flexibility to use multiple acceptor fluorophores, and the opportunity to detect sensitized acceptor emission as an easy way to measure energy transfer without the risk of also detecting donor-only signal. Here, we describe a method to use LRET on membrane proteins expressed and assayed on the surface of intact mammalian cells. We introduce a protease cleavage site between the LRET fluorophore pair. After obtaining the original LRET signal, cleavage at that site removes the specific LRET signal from the protein of interest allowing us to quantitatively subtract the background signal that remains after cleavage. This method allows for more physiologically relevant measurements to be made without the need for purification of protein.

We describe here an improved Luminescence Resonance Energy Transfer (LRET) method where we introduce a protease cleavage site between the donor and acceptor fluorophore sites. This modification allows us to obtain specific LRET signals arising from membrane proteins of interest, allowing for the study of membrane proteins without protein purification.

荧光共振能量转移研究构象变化的膜蛋白在哺乳动物细胞中表达

Luminescence Resonance Energy Transfer, or LRET, is a powerful technique used to measure distances between two sites in proteins within the distance range ...

Fluorescence-quenching of a Liposomal-encapsulated Near-infrared Fluorophore as a Tool for In Vivo Optical Imaging

Optical imaging offers a wide range of diagnostic modalities and has attracted a lot of interest as a tool for biomedical imaging. Despite the enormous number of imaging techniques currently available and the progress in instrumentation, there is still a need for highly sensitive probes that are suitable for in vivo imaging. One typical problem of available preclinical fluorescent probes is their rapid clearance in vivo, which reduces their imaging sensitivity. To circumvent rapid clearance, increase number of dye molecules at the target site, and thereby reduce background autofluorescence, encapsulation of the near-infrared fluorescent dye, DY-676-COOH in liposomes and verification of its potential for in vivo imaging of inflammation was done. DY-676 is known for its ability to self-quench at high concentrations. We first determined the concentration suitable for self-quenching, and then encapsulated this quenching concentration into the aqueous interior of PEGylated liposomes. To substantiate the quenching and activation potential of the liposomes we use a harsh freezing method which leads to damage of liposomal membranes without affecting the encapsulated dye. The liposomes characterized by a high level of fluorescence quenching were termed Lip-Q. We show by experiments with different cell lines that uptake of Lip-Q is predominantly by phagocytosis which in turn enabled the characterization of its potential as a tool for in vivo imaging of inflammation in mice models. Furthermore, we use a zymosan-induced edema model in mice to substantiate the potential of Lip-Q in optical imaging of inflammation in vivo. Considering possible uptake due to inflammation-induced enhanced permeability and retention (EPR) effect, an always-on liposome formulation with low, non-quenched concentration of DY-676-COOH (termed Lip-dQ) and the free DY-676-COOH were compared with Lip-Q in animal trials.

Fluorescence-quenching of a Liposomal-encapsulated Near-infrared Fluorophore as a Tool for In Vivo Optical Imaging

The use of fluorophores for in vivo imaging can be greatly limited by opsonization, rapid clearance, low detection sensitivity and cytotoxic effects on the host. Encapsulation of fluorophores in liposomes by film hydration and extrusion leads to fluorescence quenching and protection which enables in vivo imaging with high detection sensitivity.

荧光淬一个脂质体包封的近红外荧光团的作为一个工具<em&gt;在体内</em&gt;光学成像

Optical imaging offers a wide range of diagnostic modalities and has attracted a lot of interest as a tool for biomedical imaging. Despite the enormous ...

Sandwich-like Microenvironments to Harness Cell/Material Interactions

Cell culture has been traditionally carried out on bi-dimensional (2D) substrates where cells adhere using ventral receptors to the biomaterial surface. However in vivo, most of the cells are completely surrounded by the extracellular matrix (ECM), resulting in a three-dimensional (3D) distribution of receptors. This may trigger differences in the outside-in signaling pathways and thus in cell behavior.
This article shows that stimulating the dorsal receptors of cells already adhered to a 2D substrate by overlaying a film of a new material (a sandwich-like culture) triggers important changes with respect to standard 2D cultures. Furthermore, the simultaneous excitation of ventral and dorsal receptors shifts cell behavior closer to that found in 3D environments. Additionally, due to the nature of the system, a sandwich-like culture is a versatile tool that allows the study of different parameters in cell/material interactions, e.g., topography, stiffness and different protein coatings at both the ventral and dorsal sides. Finally, since sandwich-like cultures are based on 2D substrates, several analysis procedures already developed for standard 2D cultures can be used normally, overcoming more complex procedures needed for 3D systems.

The following protocol describes the procedure to assemble sandwich-like cultures to be used as an intermediate stage between bi-dimensional (2D) and three-dimensional (3D) cellular environments. The engineered systems can have applications in microscopy, biomechanics, biochemistry and cell biology assays.

三明治般的微环境来驾驭细胞/材料相互作用

Cell culture has been traditionally carried out on bi-dimensional (2D) substrates where cells adhere using ventral receptors to the biomaterial surface. ...

Preparation of 3D Collagen Gels and Microchannels for the Study of 3D Interactions In Vivo

Historically, most cellular processes have been studied in only 2 dimensions. While these studies have been informative about general cell signaling mechanisms, they neglect important cellular cues received from the structural and mechanical properties of the local microenvironment and extracellular matrix (ECM). To understand how cells interact within a physiological ECM, it is important to study them in the context of 3 dimensional assays. Cell migration, cell differentiation, and cell proliferation are only a few processes that have been shown to be impacted by local changes in the mechanical properties of a 3-dimensional ECM. Collagen I, a core fibrillar component of the ECM, is more than a simple structural element of a tissue. Under normal conditions, mechanical cues from the collagen network direct morphogenesis and maintain cellular structures. In diseased microenvironments, such as the tumor microenvironment, the collagen network is often dramatically remodeled, demonstrating altered composition, enhanced deposition and altered fiber organization. In breast cancer, the degree of fiber alignment is important, as an increase in aligned fibers perpendicular to the tumor boundary has been correlated to poorer patient prognosis1. Aligned collagen matrices result in increased dissemination of tumor cells via persistent migration2,3. The following is a simple protocol for embedding cells within a 3-dimensional, fibrillar collagen hydrogel. This protocol is readily adaptable to many platforms, and can reproducibly generate both aligned and random collagen matrices for investigation of cell migration, cell division, and other cellular processes in a tunable, 3-dimensional, physiological microenvironment.

Preparation of 3D Collagen Gels and Microchannels for the Study of 3D Interactions In Vivo

Collagen is a core component of the ECM, and provides essential cues for several cellular processes ranging from migration to differentiation and proliferation. Provided here is a protocol for embedding cells within 3D collagen hydrogels, and a more advanced technique for generating randomized or aligned collagen matrices using PDMS microchannels.

3D胶原凝胶和微通道3D相互作用的研究准备<em&gt;在体内</em

Historically, most cellular processes have been studied in only 2 dimensions.  While these studies have been informative about general cell signaling ...

DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers

Mechanical properties of complex, polymer-based soft matter, such as cells or biopolymer networks, can be understood in neither the classical frame of flexible polymers nor of rigid rods. Underlying filaments remain outstretched due to their non-vanishing backbone stiffness, which is quantified via the persistence length (lp), but they are also subject to strong thermal fluctuations. Their finite bending stiffness leads to unique, non-trivial collective mechanics of bulk networks, enabling the formation of stable scaffolds at low volume fractions while providing large mesh sizes. This underlying principle is prevalent in nature (e.g., in cells or tissues), minimizing the high molecular content and thereby facilitating diffusive or active transport. Due to their biological implications and potential technological applications in biocompatible hydrogels, semiflexible polymers have been subject to considerable study. However, comprehensible investigations remained challenging since they relied on natural polymers, such as actin filaments, which are not freely tunable. Despite these limitations and due to the lack of synthetic, mechanically tunable, and semiflexible polymers, actin filaments were established as the common model system. A major limitation is that the central quantity lp cannot be freely tuned to study its impact on macroscopic bulk structures. This limitation was resolved by employing structurally programmable DNA nanotubes, enabling controlled alteration of the filament stiffness. They are formed through tile-based designs, where a discrete set of partially complementary strands hybridize in a ring structure with a discrete circumference. These rings feature sticky ends, enabling the effective polymerization into filaments several microns in length, and display similar polymerization kinetics as natural biopolymers. Due to their programmable mechanics, these tubes are versatile, novel tools to study the impact of lp on the single-molecule as well as the bulk scale. In contrast to actin filaments, they remain stable over weeks, without notable degeneration, and their handling is comparably straightforward.

Semiflexible polymers display unique mechanical properties that are extensively applied by living systems. However, systematic studies on biopolymers are limited since properties such as polymer rigidity are inaccessible. This manuscript describes how this limitation is circumvented by programmable DNA nanotubes, enabling experimental studies on the impact of filament rigidity.

DNA 纳米管作为研究半聚合物的万能工具

Mechanical properties of complex, polymer-based soft matter, such as cells or biopolymer networks, can be understood in neither the classical frame of ...

Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics

Proteases are multi-functional enzymes that specialize in the hydrolysis of peptide-bonds and control broad biological processes including homeostasis and allostasis. Moreover, dysregulated protease activity drives pathogenesis and is a functional biomarker of diseases such as cancer; therefore, the ability to detect protease activity in vivo may provide clinically relevant information for biomedical diagnostics. The goal of this protocol is to create nanosensors that probe for protease activity in vivo by producing a quantifiable signal in urine. These protease nanosensors consist of two components: a nanoparticle and substrate. The nanoparticle functions to increase circulation half-life and substrate delivery to target disease sites. The substrate is a short peptide sequence (6-8 AA), which is designed to be specific to a target protease or group of proteases. The substrate is conjugated to the surface of the nanoparticle and is terminated by a reporter, such as a fluorescent marker, for detection. As dysregulated proteases cleave the peptide substrate, the reporter is filtered into urine for quantification as a biomarker of protease activity. Herein we describe construction of a nanosensor for matrix metalloproteinase 9 (MMP9), which is associated with tumor progression and metastasis, for detection of colorectal cancer in a mouse model.

Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics

Proteases are tightly regulated enzymes involved in fundamental biological processes, and dysregulated protease activity drives progression of complex diseases such as cancer. This method&#39;s goal is to create nanosensors that measure protease activity in vivo by producing a cleavage signal that is detectable from host urine and discriminates disease.

纳米传感器检测体内蛋白酶活性的无创诊断

Proteases are multi-functional enzymes that specialize in the hydrolysis of peptide-bonds and control broad biological processes including homeostasis and ...

膜脊柱:一个生化工具来确定膜蛋白的蛋白质 - 蛋白质相互作用

摘要

探索更多视频

此视频中的章节