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本文引用的文献

1
Three-dimensional structure of a viral genome-delivery portal vertex.病毒基因组递送门顶点的三维结构。
Nat Struct Mol Biol. 2011 May;18(5):597-603. doi: 10.1038/nsmb.2023. Epub 2011 Apr 17.
2
Structural basis for scaffolding-mediated assembly and maturation of a dsDNA virus.支架介导的双链 DNA 病毒组装和成熟的结构基础。
Proc Natl Acad Sci U S A. 2011 Jan 25;108(4):1355-60. doi: 10.1073/pnas.1015739108. Epub 2011 Jan 10.
3
The CRISPR/Cas bacterial immune system cleaves bacteriophage and plasmid DNA.CRISPR/Cas 细菌免疫系统可切割噬菌体和质粒 DNA。
Nature. 2010 Nov 4;468(7320):67-71. doi: 10.1038/nature09523.
4
Structure and molecular assignment of lactococcal phage TP901-1 baseplate.乳球菌噬菌体 TP901-1 基板的结构与分子分配。
J Biol Chem. 2010 Dec 10;285(50):39079-86. doi: 10.1074/jbc.M110.175646. Epub 2010 Oct 11.
5
Crystal structure of bacteriophage SPP1 distal tail protein (gp19.1): a baseplate hub paradigm in gram-positive infecting phages.噬菌体 SPP1 远端尾部蛋白(gp19.1)的晶体结构:革兰氏阳性侵染噬菌体的基板中心体范例。
J Biol Chem. 2010 Nov 19;285(47):36666-73. doi: 10.1074/jbc.M110.157529. Epub 2010 Sep 15.
6
The solution structure of the C-terminal Ig-like domain of the bacteriophage λ tail tube protein.噬菌体 λ 尾管蛋白 C 端 Ig 样结构域的溶液结构。
J Mol Biol. 2010 Oct 29;403(3):468-79. doi: 10.1016/j.jmb.2010.08.044. Epub 2010 Sep 6.
7
Phages have adapted the same protein fold to fulfill multiple functions in virion assembly.噬菌体已经适应了相同的蛋白质折叠,以在病毒组装中发挥多种功能。
Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14384-9. doi: 10.1073/pnas.1005822107. Epub 2010 Jul 26.
8
Length control of the injectisome needle requires only one molecule of Yop secretion protein P (YscP).注入体针的长度控制仅需要一个 Yop 分泌蛋白 P(YscP)分子。
Proc Natl Acad Sci U S A. 2010 Aug 3;107(31):13860-5. doi: 10.1073/pnas.1006985107. Epub 2010 Jul 19.
9
Structural changes in a marine podovirus associated with release of its genome into Prochlorococcus.与海洋 Podovirus 基因组释放有关的结构变化。
Nat Struct Mol Biol. 2010 Jul;17(7):830-6. doi: 10.1038/nsmb.1823. Epub 2010 Jun 13.
10
The tripartite capsid gene of Salmonella phage Gifsy-2 yields a capsid assembly pathway engaging features from HK97 and lambda.肠炎沙门氏菌噬菌体 Gifsy-2 的三分基因组编码一个衣壳组装途径,涉及 HK97 和 lambda 的特征。
Virology. 2010 Jul 5;402(2):355-65. doi: 10.1016/j.virol.2010.03.041. Epub 2010 Apr 28.

尾部噬菌体功能模块和细菌机器的共同进化起源。

A common evolutionary origin for tailed-bacteriophage functional modules and bacterial machineries.

机构信息

Architecture et Fonction des Macromolécules Biologiques (AFMB), UMR 6098 CNRS, and Universités Aix-Marseille I & II, Campus de Luminy, Case 932, 13288 Marseille Cedex 09, France.

出版信息

Microbiol Mol Biol Rev. 2011 Sep;75(3):423-33, first page of table of contents. doi: 10.1128/MMBR.00014-11.

DOI:10.1128/MMBR.00014-11
PMID:21885679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165541/
Abstract

Bacteriophages belonging to the order Caudovirales possess a tail acting as a molecular nanomachine used during infection to recognize the host cell wall, attach to it, pierce it, and ensure the high-efficiency delivery of the genomic DNA to the host cytoplasm. In this review, we provide a comprehensive analysis of the various proteins constituting tailed bacteriophages from a structural viewpoint. To this end, we had in mind to pinpoint the resemblances within and between functional modules such as capsid/tail connectors, the tails themselves, or the tail distal host recognition devices, termed baseplates. This comparison has been extended to bacterial machineries embedded in the cell wall, for which shared molecular homology with phages has been recently revealed. This is the case for the type VI secretion system (T6SS), an inverted phage tail at the bacterial surface, or bacteriocins. Gathering all these data, we propose that a unique ancestral protein fold may have given rise to a large number of bacteriophage modules as well as to some related bacterial machinery components.

摘要

噬菌体属于长尾病毒目,它们的尾巴充当分子纳米机器,在感染过程中用于识别宿主细胞壁,附着在细胞壁上,刺穿细胞壁,并确保基因组 DNA 高效递送至宿主细胞质。在这篇综述中,我们从结构角度对构成长尾噬菌体的各种蛋白质进行了全面分析。为此,我们旨在确定壳/尾连接物、尾巴本身或称为基板的尾部远端宿主识别装置等功能模块内和模块之间的相似性。这种比较已经扩展到嵌入细胞壁的细菌机器,最近发现噬菌体与这些细菌机器具有共享的分子同源性。这种情况适用于位于细菌表面的反转噬菌体尾部的 VI 型分泌系统 (T6SS) 或细菌素。收集所有这些数据后,我们提出一个独特的祖先蛋白折叠可能产生了大量的噬菌体模块以及一些相关的细菌机器组件。