Suppr超能文献

维持整合膜蛋白质组:重新审视整合膜蛋白酶的功能库。

Maintaining the Integral Membrane Proteome: Revisiting the Functional Repertoire of Integral Membrane Proteases.

作者信息

Fremlén Hannah, Burmann Björn M

机构信息

Department of Chemistry and Molecular Biology, Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, 405 30, Göteborg, Sweden.

Department of Chemistry and Molecular Biology, Wallenberg Centre for Molecular and Translational Medicine, Science for Life Laboratory, Swedish NMR Centre, University of Gothenburg, 405 30, Göteborg, Sweden.

出版信息

Chembiochem. 2025 May 5;26(9):e202500048. doi: 10.1002/cbic.202500048. Epub 2025 Mar 18.

Abstract

Cells in all kingdoms of life employ dedicated protein quality control machineries for both their cytosolic and membrane proteome ensuring cellular functionality. These crucial systems consist besides a large variety of molecular chaperones, ensuring a proper fold and consequently function of the client's proteome, of several proteases to clean out damaged, unfunctional and potentially toxic proteins. One of the key features underlying the functional cycle of these quality control systems is the inherent flexibility of their bound clients which for a long time impaired detailed structural characterization, with advanced high-resolution NMR spectroscopy in the last decade playing a key role contributing to the present understanding of their functional properties. Although these studies laid the foundation of the present knowledge of the mechanistic details of the maintenance of cytosolic proteins, the understanding of related systems employed for membrane associated as well as integral membrane proteins remains rather sparse to date. Herein, we review the crucial contributions of structural and dynamical biology approaches, possessing the power to resolve both structure and dynamics of such systems as well as enabling the elucidation of the functional repertoire of multimeric proteases involved in maintaining a functional membrane proteome.

摘要

所有生命王国中的细胞都利用专门的蛋白质质量控制机制来维持其胞质和膜蛋白质组,以确保细胞功能。这些关键系统除了包含多种分子伴侣(确保客户蛋白质组正确折叠并进而发挥功能)外,还包括几种蛋白酶,用于清除受损、无功能和潜在有毒的蛋白质。这些质量控制系统功能循环的一个关键特征是其结合客户的固有灵活性,长期以来这阻碍了详细的结构表征,在过去十年中,先进的高分辨率核磁共振光谱在促进目前对其功能特性的理解方面发挥了关键作用。尽管这些研究为目前关于胞质蛋白维持机制细节的知识奠定了基础,但迄今为止,对用于膜相关蛋白以及整合膜蛋白的相关系统的了解仍然相当匮乏。在此,我们回顾结构和动态生物学方法的重要贡献,这些方法有能力解析此类系统的结构和动态,还能阐明参与维持功能性膜蛋白质组的多聚体蛋白酶的功能库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac23/12067869/cbaf979196c8/CBIC-26-e202500048-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验