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噬菌体和相关系统的收缩注射系统。

Contractile injection systems of bacteriophages and related systems.

机构信息

Structural Biology of Molecular Machines Group, Protein Structure & Function Programme, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen 2200, Denmark.

Departamento de Estructura de Macromoleculas, Centro Nacional de Biotecnologia (CSIC), Calle Darwin 3, E-28049 Madrid, Spain.

出版信息

Mol Microbiol. 2018 Apr;108(1):6-15. doi: 10.1111/mmi.13921. Epub 2018 Feb 26.

Abstract

Contractile tail bacteriophages, or myobacteriophages, use a sophisticated biomolecular structure to inject their genome into the bacterial host cell. This structure consists of a contractile sheath enveloping a rigid tube that is sharpened by a spike-shaped protein complex at its tip. The spike complex forms the centerpiece of a baseplate complex that terminates the sheath and the tube. The baseplate anchors the tail to the target cell membrane with the help of fibrous proteins emanating from it and triggers contraction of the sheath. The contracting sheath drives the tube with its spiky tip through the target cell membrane. Subsequently, the bacteriophage genome is injected through the tube. The structural transformation of the bacteriophage T4 baseplate upon binding to the host cell has been recently described in near-atomic detail. In this review we discuss structural elements and features of this mechanism that are likely to be conserved in all contractile injection systems (systems evolutionary and structurally related to contractile bacteriophage tails). These include the type VI secretion system (T6SS), which is used by bacteria to transfer effectors into other bacteria and into eukaryotic cells, and tailocins, a large family of contractile bacteriophage tail-like compounds that includes the P. aeruginosa R-type pyocins.

摘要

收缩尾噬菌体,或分枝杆菌噬菌体,利用一种复杂的生物分子结构将其基因组注入细菌宿主细胞。这个结构由一个收缩鞘包裹着一个刚性管组成,在其尖端由一个刺状蛋白复合物来加强。刺状复合物形成了底盘复合物的中心部分,底盘复合物终止了鞘和管。底盘借助从它发出的纤维状蛋白质将尾巴固定在靶细胞膜上,并触发鞘的收缩。收缩的鞘带动带有刺的管穿过靶细胞膜。随后,噬菌体基因组通过管被注入。最近已经详细描述了噬菌体 T4 底盘与宿主细胞结合时的结构转变。在这篇综述中,我们讨论了这个机制的结构元素和特征,这些特征很可能在所有收缩注入系统(与收缩噬菌体尾巴在进化和结构上相关的系统)中保守。这些系统包括用于细菌将效应蛋白转移到其他细菌和真核细胞中的六型分泌系统(T6SS),以及一大类收缩噬菌体尾样化合物尾丝菌素,其中包括铜绿假单胞菌 R 型 pyocins。

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