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AAA+蛋白Msp1通过疏水错配识别底物。

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

作者信息

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

机构信息

Previously at University of Toledo, Department of Chemistry & Biochemistry.

University of Pittsburgh, Department of Cell Biology.

出版信息

bioRxiv. 2024 Sep 29:2023.07.11.548587. doi: 10.1101/2023.07.11.548587.

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.

摘要

蛋白质质量控制的一个重要方面是从脂质双层中酶促去除膜蛋白。这一基本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+(与多种细胞活动相关的ATP酶)蛋白,可从线粒体外膜(OMM)中去除错误定位的蛋白。Msp1如何在复杂的OMM生态系统中选择性识别和提取底物,以及脂质双层在这些过程中的作用尚不清楚。在这里,我们描述了一种完全定义的、快速且定量的提取测定方法的开发,该方法保留了生理底物选择性。使用这种新方法,我们系统地改变了底物和脂质环境,以证明Msp1通过底物跨膜结构域(TMD)与脂质双层之间的疏水错配来识别底物。我们进一步证明,Msp1活性的限速步骤是TMD从脂质双层中的提取。这些结果共同为脂质双层如何影响AAA+介导的膜蛋白提取提供了基础见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/915b/11455580/34d639d5b121/nihpp-2023.07.11.548587v2-f0001.jpg

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