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荧光相关光谱法:检测和解读体内跨膜蛋白的流动性

Fluorescence correlation spectroscopy: detecting and interpreting the mobility of transmembrane proteins in vivo.

作者信息

Malchus Nina

机构信息

German Cancer Research Center, Heidelberg, Germany.

出版信息

Curr Protoc Toxicol. 2011 May;Chapter 2:Unit2.19. doi: 10.1002/0471140856.tx0219s48.

Abstract

Mobility of proteins is crucial for their functionality. Fluorescence correlation spectroscopy (FCS) is a sensitive tool for assessing dynamics in vivo. It can reveal properties of diffusing proteins, as well as of the surrounding medium. Hence, subtle changes in the dynamics after treatment with toxic substances can be visualized. On biological membranes, the high concentration of transmembrane and peripheral membrane proteins leads to molecular crowding, and thus to a change in the diffusion behavior, i.e., to anomalous diffusion of membrane proteins. Presented here is a protocol for conducting and evaluating FCS measurements of membrane proteins before and after treatment.

摘要

蛋白质的流动性对其功能至关重要。荧光相关光谱法(FCS)是一种评估体内动力学的灵敏工具。它可以揭示扩散蛋白以及周围介质的特性。因此,用有毒物质处理后动力学的细微变化可以可视化。在生物膜上,跨膜蛋白和外周膜蛋白的高浓度导致分子拥挤,从而导致扩散行为的改变,即膜蛋白的反常扩散。本文介绍了一种在处理前后进行和评估膜蛋白FCS测量的方案。

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