Single-Molecule Force Spectroscopy of Membrane Protein Folding

被引:6
|
作者
Wijesinghe, W. C. Bhashini [1 ]
Min, Duyoung [1 ,2 ]
机构
[1] Ulsan Natl Inst Sci & Technol UNIST, Dept Chem, Ulsan 44919, South Korea
[2] Ulsan Natl Inst Sci & Technol UNIST, Ctr Wave Energy Mat, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
AFM; magnetic tweezers; forced unfolding; refolding; lipid bilayers; SODIUM-PROTON ANTIPORTER; ONE BETA-HAIRPIN; ENERGY LANDSCAPE; OUTER-MEMBRANE; UNFOLDING PATHWAYS; MECHANICAL-PROPERTIES; OPTICAL TWEEZERS; BACTERIORHODOPSIN; STABILITY; RHODOPSIN;
D O I
10.1016/j.jmb.2023.167975
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single-molecule force spectroscopy is a unique method that can probe the structural changes of single proteins at a high spatiotemporal resolution while mechanically manipulating them over a wide force range. Here, we review the current understanding of membrane protein folding learned by using the force spectroscopy approach. Membrane protein folding in lipid bilayers is one of the most complex biological processes in which diverse lipid molecules and chaperone proteins are intricately involved. The approach of single protein forced unfolding in lipid bilayers has produced important findings and insights into mem-brane protein folding. This review provides an overview of the forced unfolding approach, including recent achievements and technical advances. Progress in the methods can reveal more interesting cases of membrane protein folding and clarify general mechanisms and principles.& COPY; 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:25
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