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本文引用的文献

1
Intracellular bacteria encode inhibitory SNARE-like proteins.细胞内细菌编码抑制性 SNARE 样蛋白。
PLoS One. 2009 Oct 12;4(10):e7375. doi: 10.1371/journal.pone.0007375.
2
Leading a sheltered life: intracellular pathogens and maintenance of vacuolar compartments.过着受保护的生活:细胞内病原体与液泡区室的维持
Cell Host Microbe. 2009 Jun 18;5(6):593-601. doi: 10.1016/j.chom.2009.05.014.
3
Legionella eukaryotic-like type IV substrates interfere with organelle trafficking.嗜肺军团菌真核样IV型底物干扰细胞器运输。
PLoS Pathog. 2008 Aug 1;4(8):e1000117. doi: 10.1371/journal.ppat.1000117.
4
SNARE protein mimicry by an intracellular bacterium.一种细胞内细菌对SNARE蛋白的模拟
PLoS Pathog. 2008 Mar 14;4(3):e1000022. doi: 10.1371/journal.ppat.1000022.
5
Manipulation of rab GTPase function by intracellular bacterial pathogens.细胞内细菌病原体对小GTP酶功能的操控。
Microbiol Mol Biol Rev. 2007 Dec;71(4):636-52. doi: 10.1128/MMBR.00023-07.
6
The role of protein secretion systems in the virulence of the intracellular pathogen Legionella pneumophila.蛋白质分泌系统在细胞内病原体嗜肺军团菌毒力中的作用。
Microbiology (Reading). 2007 Dec;153(Pt 12):3948-3953. doi: 10.1099/mic.0.2007/012039-0.
7
Legionella pneumophila proteins that regulate Rab1 membrane cycling.调节Rab1膜循环的嗜肺军团菌蛋白质。
Nature. 2007 Nov 15;450(7168):365-9. doi: 10.1038/nature06336. Epub 2007 Oct 21.
8
SNAREing immunity: the role of SNAREs in the immune system.SNARE蛋白与免疫:SNARE蛋白在免疫系统中的作用
Nat Rev Immunol. 2006 Dec;6(12):919-29. doi: 10.1038/nri1980.
9
Crystal structures of Nipah and Hendra virus fusion core proteins.尼帕病毒和亨德拉病毒融合核心蛋白的晶体结构
FEBS J. 2006 Oct;273(19):4538-47. doi: 10.1111/j.1742-4658.2006.05459.x.
10
The Legionella pneumophila effector protein DrrA is a Rab1 guanine nucleotide-exchange factor.嗜肺军团菌效应蛋白DrrA是一种Rab1鸟嘌呤核苷酸交换因子。
Nat Cell Biol. 2006 Sep;8(9):971-7. doi: 10.1038/ncb1463. Epub 2006 Aug 13.

SNARE 基序:病原体用来操纵膜融合的常见基序。

SNARE motif: a common motif used by pathogens to manipulate membrane fusion.

机构信息

Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA, USA.

出版信息

Virulence. 2010 Jul-Aug;1(4):319-24. doi: 10.4161/viru.1.4.12195.

DOI:10.4161/viru.1.4.12195
PMID:21178463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3073298/
Abstract

To penetrate host cells through their membranes, pathogens use a variety of molecular components in which the presence of heptad repeat motifs seems to be a prevailing element. Heptad repeats are characterized by a pattern of seven, generally hydrophobic, residues. In order to initiate membrane fusion, viruses use glycoproteins-containing heptad repeats. These proteins are structurally and functionally similar to the SNARE proteins known to be involved in eukaryotic membrane fusion. SNAREs also display a heptad repeat motif called the "SNARE motif". As bacterial genomes are being sequenced, microorganisms also appear to be carrying membrane proteins resembling eukaryotic SNAREs. This category of SNARE-like proteins might share similar functions and could be used by microorganisms to either promote or block membrane fusion. Such a recurrence across pathogenic organisms suggests that this architectural motif was evolutionarily selected because it most effectively ensures the survival of pathogens within the eukaryotic environment.

摘要

为了穿透宿主细胞的细胞膜,病原体使用了多种分子成分,其中七肽重复基序的存在似乎是一个主要元素。七肽重复基序的特征是具有一种七肽重复模式,通常是疏水性残基。为了启动膜融合,病毒使用含有七肽重复基序的糖蛋白。这些蛋白质在结构和功能上与真核生物膜融合中已知的 SNARE 蛋白相似。SNARE 蛋白也显示出一种七肽重复基序,称为“SNARE 基序”。随着细菌基因组的测序,微生物似乎也携带类似于真核 SNARE 的膜蛋白。这一类 SNARE 样蛋白可能具有相似的功能,并可被微生物用来促进或阻止膜融合。这种在病原体中的反复出现表明,这种结构基序是通过进化选择的,因为它最有效地确保了病原体在真核环境中的生存。