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分枝杆菌中蛋白质破坏的AAA+机器

AAA+ Machines of Protein Destruction in Mycobacteria.

作者信息

Alhuwaider Adnan Ali H, Dougan David A

机构信息

Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe UniversityMelbourne, VIC, Australia.

出版信息

Front Mol Biosci. 2017 Jul 19;4:49. doi: 10.3389/fmolb.2017.00049. eCollection 2017.

Abstract

The bacterial cytosol is a complex mixture of macromolecules (proteins, DNA, and RNA), which collectively are responsible for an enormous array of cellular tasks. Proteins are central to most, if not all, of these tasks and as such their maintenance (commonly referred to as protein homeostasis or proteostasis) is vital for cell survival during normal and stressful conditions. The two key aspects of protein homeostasis are, (i) the correct folding and assembly of proteins (coupled with their delivery to the correct cellular location) and (ii) the timely removal of unwanted or damaged proteins from the cell, which are performed by molecular chaperones and proteases, respectively. A major class of proteins that contribute to both of these tasks are the AAA+ (ATPases associated with a variety of cellular activities) protein superfamily. Although much is known about the structure of these machines and how they function in the model Gram-negative bacterium , we are only just beginning to discover the molecular details of these machines and how they function in mycobacteria. Here we review the different AAA+ machines, that contribute to proteostasis in mycobacteria. Primarily we will focus on the recent advances in the structure and function of AAA+ proteases, the substrates they recognize and the cellular pathways they control. Finally, we will discuss the recent developments related to these machines as novel drug targets.

摘要

细菌胞质溶胶是由大分子(蛋白质、DNA和RNA)组成的复杂混合物,这些大分子共同负责大量的细胞任务。蛋白质对于大多数(如果不是全部)这些任务都至关重要,因此它们的维持(通常称为蛋白质稳态或蛋白质平衡)对于细胞在正常和应激条件下的存活至关重要。蛋白质稳态的两个关键方面是:(i)蛋白质的正确折叠和组装(以及将它们递送到正确的细胞位置),以及(ii)及时从细胞中清除不需要的或受损的蛋白质,这分别由分子伴侣和蛋白酶执行。对这两项任务都有贡献的一大类蛋白质是AAA+(与多种细胞活动相关的ATP酶)蛋白质超家族。尽管我们对这些机器的结构以及它们在模式革兰氏阴性菌中的功能了解很多,但我们才刚刚开始发现这些机器的分子细节以及它们在分枝杆菌中的功能。在这里,我们综述了有助于分枝杆菌蛋白质稳态的不同AAA+机器。主要我们将关注AAA+蛋白酶的结构和功能、它们识别的底物以及它们控制的细胞途径方面的最新进展。最后,我们将讨论与这些机器作为新型药物靶点相关的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f301/5515868/8adc926b3aa8/fmolb-04-00049-g0001.jpg

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