Structural biology of type VI secretion systems

被引:178
作者
Cascales, Eric [1 ]
Cambillau, Christian [2 ,3 ]
机构
[1] Aix Marseille Univ, Inst Microbiol Mediterranee, CNRS, Lab Ingn Syst Macromol,UMR 7255, F-13402 Marseille 20, France
[2] Aix Marseille Univ, F-13288 Marseille 09, France
[3] CNRS, UMR 6098, F-13288 Marseille 09, France
关键词
protein transport; protein trafficking; bacteriophage; secretion; Hcp; VgrG; VIBRIO-CHOLERAE; CRYSTAL-STRUCTURE; TAILED PHAGES; PROTEIN; BACTERIOPHAGE-T4; BASEPLATE; IDENTIFICATION; COMPONENT; MECHANISM; REVEALS;
D O I
10.1098/rstb.2011.0209
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Type VI secretion systems (T6SSs) are transenvelope complexes specialized in the transport of proteins or domains directly into target cells. These systems are versatile as they can target either eukaryotic host cells and therefore modulate the bacteria-host interaction and pathogenesis or bacterial cells and therefore facilitate access to a specific niche. These molecular machines comprise at least 13 proteins. Although recent years have witnessed advances in the role and function of these secretion systems, little is known about how these complexes assemble in the cell envelope. Interestingly, the current information converges to the idea that T6SSs are composed of two subassemblies, one resembling the contractile bacteriophage tail, whereas the other subunits are embedded in the inner and outer membranes and anchor the bacteriophage-like structure to the cell envelope. In this review, we summarize recent structural information on individual T6SS components emphasizing the fact that T6SSs are composite systems, adapting subunits from various origins.
引用
收藏
页码:1102 / 1111
页数:10
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