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{"title":"In vitro Assays for Targeting and Insertion of Tail-Anchored Proteins Into the ER Membrane","authors":"Hyunju Cho, Un Seng Chio, Shu-ou Shan","doi":"10.1002/cpcb.63","DOIUrl":null,"url":null,"abstract":"<p>Membrane proteins mediate numerous essential cellular functions. Due to the aggregation propensity of hydrophobic transmembrane domains in aqueous environments, the targeting and insertion of membrane proteins pose major challenges to cells. In the Guided Entry of Tail-anchored protein (GET) pathway, an essential class of newly synthesized tail-anchored proteins (TAs) are chaperoned and guided by multiple targeting factors to the endoplasmic reticulum (ER) membrane. Deciphering the molecular mechanism of this cellular process has benefitted from successful <i>in vitro</i> reconstitution of individual molecular events in the GET pathway with purified components. Here we describe recently developed protocols for <i>in vitro</i> reconstitution of functional complexes of TA substrates with their targeting factors, for monitoring the transfer of TAs between targeting factors, and for the insertion of TA into the microsomal membrane. These procedures are generally applicable to the interrogation of other post-translational membrane protein targeting pathways. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":40051,"journal":{"name":"Current Protocols in Cell Biology","volume":"81 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcb.63","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcb.63","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
Membrane proteins mediate numerous essential cellular functions. Due to the aggregation propensity of hydrophobic transmembrane domains in aqueous environments, the targeting and insertion of membrane proteins pose major challenges to cells. In the Guided Entry of Tail-anchored protein (GET) pathway, an essential class of newly synthesized tail-anchored proteins (TAs) are chaperoned and guided by multiple targeting factors to the endoplasmic reticulum (ER) membrane. Deciphering the molecular mechanism of this cellular process has benefitted from successful in vitro reconstitution of individual molecular events in the GET pathway with purified components. Here we describe recently developed protocols for in vitro reconstitution of functional complexes of TA substrates with their targeting factors, for monitoring the transfer of TAs between targeting factors, and for the insertion of TA into the microsomal membrane. These procedures are generally applicable to the interrogation of other post-translational membrane protein targeting pathways. © 2018 by John Wiley & Sons, Inc.
尾锚定蛋白在内质网膜中的靶向和插入的体外实验
膜蛋白介导许多基本的细胞功能。由于疏水跨膜结构域在水环境中的聚集倾向,膜蛋白的靶向和插入对细胞构成了重大挑战。在尾巴锚定蛋白(GET)通路中,一类新合成的尾巴锚定蛋白(TAs)在多种靶向因子的陪同和引导下到达内质网(ER)膜。破译这一细胞过程的分子机制得益于GET途径中单个分子事件的体外成功重构。在这里,我们描述了最近开发的方案,用于TA底物与其靶向因子的功能复合物的体外重构,用于监测TA在靶向因子之间的转移,以及用于TA插入微粒体膜。这些程序一般适用于其他翻译后膜蛋白靶向途径的询问。©2018 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。