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人P-糖蛋白构象变化的活细胞荧光共振能量转移分析

Live Cell FRET Analysis of the Conformational Changes of Human P-glycoprotein.

作者信息

Futamata Ryota, Kioka Noriyuki, Ueda Kazumitsu

机构信息

Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.

Institute for Integrated Cell-Material Sciences (WPI-iCeMS), KUIAS, Kyoto University, Kyoto 606-8501, Japan.

出版信息

Bio Protoc. 2021 Feb 20;11(4):e3930. doi: 10.21769/BioProtoc.3930.

Abstract

The molecular mechanisms of P-glycoprotein (P-gp; also known as MDR1 or ABCB1) have been mainly investigated using artificial membranes such as lipid-detergent mixed micelles, artificial lipid bilayers, and membrane vesicles derived from cultured cells. Although these experiments help illustrate details about the molecular mechanisms of P-gp, they do not reflect physiological membrane environments in terms of lateral pressure, curvature, constituent lipid species, The protocol presented here includes a detailed guide for analyzing the conformational change of human P-gp in living HEK293 cells by using intramolecular fluorescence resonance energy transfer (FRET), in which excitation of the donor fluorophore is transferred to the acceptor without emission of a photon when two fluorescent proteins are in close proximity. Combining FRET analysis with membrane permeabilization, the contribution of small molecules such as nucleotides to the conformational change can be evaluated in living cells.

摘要

P-糖蛋白(P-gp;也称为MDR1或ABCB1)的分子机制主要是利用人工膜进行研究的,如脂质去污剂混合胶束、人工脂质双层以及源自培养细胞的膜囊泡。尽管这些实验有助于阐明P-gp分子机制的细节,但就侧向压力、曲率、组成脂质种类而言,它们并不能反映生理膜环境。本文介绍的方案包括一个详细指南,用于通过分子内荧光共振能量转移(FRET)分析活的HEK293细胞中人P-gp的构象变化,当两个荧光蛋白靠得很近时,供体荧光团的激发会在不发射光子的情况下转移到受体。将FRET分析与膜通透化相结合,可以在活细胞中评估核苷酸等小分子对构象变化的贡献。

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