Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine in St. Louis, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine in St. Louis, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
J Mol Biol. 2021 Aug 6;433(16):167103. doi: 10.1016/j.jmb.2021.167103. Epub 2021 Jun 15.
The synthesis, folding, and function of membrane transport proteins are critical factors for defining cellular physiology. Since the stability of these proteins evolved amidst the lipid bilayer, it is no surprise that we are finding that many of these membrane proteins demonstrate coupling of their structure or activity in some way to the membrane. More and more transporter structures are being determined with some information about the surrounding membrane, and computational modeling is providing further molecular details about these solvation structures. Thus, the field is moving towards identifying which molecular mechanisms - lipid interactions, membrane perturbations, differential solvation, and bulk membrane effects - are involved in linking membrane energetics to transporter stability and function. In this review, we present an overview of these mechanisms and the growing evidence that the lipid bilayer is a major determinant of the fold, form, and function of membrane transport proteins in membranes.
膜转运蛋白的合成、折叠和功能是定义细胞生理学的关键因素。由于这些蛋白质的稳定性是在脂质双层中进化而来的,因此毫不奇怪,我们发现许多膜蛋白的结构或活性以某种方式与膜偶联。越来越多的转运蛋白结构被确定,同时也获得了一些关于周围膜的信息,计算建模则进一步提供了这些溶剂化结构的分子细节。因此,该领域正在努力确定哪些分子机制(脂质相互作用、膜扰动、差异溶剂化和整体膜效应)参与将膜能量与转运蛋白稳定性和功能联系起来。在这篇综述中,我们概述了这些机制以及越来越多的证据表明,脂质双层是膜转运蛋白在膜中的折叠、形式和功能的主要决定因素。