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ER/K-link-利用天然蛋白连接子探测动态细胞相互作用。

ER/K-link-Leveraging a native protein linker to probe dynamic cellular interactions.

机构信息

Department of Genetics, Cell Biology, and Development, College of Biological Sciences, University of Minnesota, Minneapolis, MN, United States.

Department of Genetics, Cell Biology, and Development, College of Biological Sciences, University of Minnesota, Minneapolis, MN, United States.

出版信息

Methods Enzymol. 2021;647:173-208. doi: 10.1016/bs.mie.2020.10.002. Epub 2020 Nov 18.

Abstract

ER/K α-helices are a subset of single alpha helical domains, which exhibit unusual stability as isolated protein secondary structures. They adopt an elongated structural conformation, while regulating the frequency of interactions between proteins or polypeptides fused to their ends. Here we review recent advances on the structure, stability and function of ER/K α-helices as linkers (ER/K linkers) in native proteins. We describe methodological considerations in the molecular cloning, protein expression and measurement of interaction strengths, using sensors incorporating ER/K linkers. We highlight biological insights obtained over the last decade by leveraging distinct biophysical features of ER/K-linked sensors. We conclude with the outlook for the use of ER/K linkers in the selective modulation of dynamic cellular interactions.

摘要

内质网/高尔基 K α-螺旋是单 α 螺旋结构域的一个子集,作为独立的蛋白质二级结构,它们表现出异常的稳定性。它们采用拉长的结构构象,同时调节与其末端融合的蛋白质或多肽之间相互作用的频率。在这里,我们综述了内质网/高尔基 K α-螺旋作为天然蛋白质连接子(内质网/高尔基连接子)的结构、稳定性和功能的最新进展。我们描述了在分子克隆、蛋白质表达和相互作用强度测量中使用包含内质网/高尔基连接子的传感器的方法学考虑因素。我们强调了过去十年中利用内质网/高尔基连接子传感器的独特生物物理特性获得的生物学见解。最后,我们展望了内质网/高尔基连接子在选择性调节动态细胞相互作用中的应用。

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