The AAA+ protein Msp1 recognizes substrates by a hydrophobic mismatch.

Heidi L Fresenius, Deepika Gaur, Baylee Smith, Brian Acquaviva, Matthew L Wohlever
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Abstract

An essential aspect of protein quality control is enzymatic removal of membrane proteins from the lipid bilayer. Failures in this essential cellular process are associated with neurodegenerative diseases and cancer. Msp1 is a AAA+ (ATPases Associated with diverse cellular Activities) protein that removes mistargeted proteins from the outer mitochondrial membrane (OMM). How Msp1 selectively recognizes and extracts substrates within the complex OMM ecosystem, and the role of the lipid bilayer on these processes is unknown. Here, we describe the development of fully defined, rapid, and quantitative extraction assay that retains physiological substrate selectivity. Using this new assay, we systematically modified both substrates and the lipid environment to demonstrate that Msp1 recognizes substrates by a hydrophobic mismatch between the substrate TMD and the lipid bilayer. We further demonstrate that the rate limiting step in Msp1 activity is extraction of the TMD from the lipid bilayer. Together, these results provide foundational insights into how the lipid bilayer influences AAA+ mediated membrane protein extraction.

AAA+ 蛋白质 Msp1 通过疏水错配识别底物。
蛋白质质量控制的一个重要方面是通过酶从脂质双分子层中去除膜蛋白。这一重要细胞过程的失败与神经退行性疾病和癌症有关。Msp1 是一种 AAA+(与多种细胞活动有关的 ATPases)蛋白,它能从线粒体外膜(OMM)上清除目标错误的蛋白质。Msp1 如何在复杂的线粒体外膜生态系统中选择性地识别和提取底物,以及脂质双分子层在这些过程中的作用尚不清楚。在这里,我们描述了完全定义、快速和定量提取测定的发展,它保留了生理底物选择性。利用这种新的检测方法,我们系统地改变了底物和脂质环境,证明 Msp1 是通过底物 TMD 与脂质双分子层之间的疏水错配来识别底物的。我们进一步证明,Msp1 活性的限速步骤是从脂质双分子层中提取 TMD。这些结果为我们深入了解脂质双分子层如何影响 AAA+ 介导的膜蛋白提取提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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