期刊
NATURE
卷 540, 期 7634, 页码 597-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature20576
关键词
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资金
- Canadian Institutes of Health Research (CIHR)
- Michael Smith Foundation of Health Research
- CIHR
- Howard Hughes International Senior Scholar program
- Canada Research Chair in Antibiotic Discovery
The type III secretion (T3S) injectisome is a specialized protein nanomachine that is critical for the pathogenicity of many Gram-negative bacteria, including purveyors of plague, typhoid fever, whooping cough, sexually transmitted infections and major nosocomial infections. This syringe-shaped 3.5-MDa macromolecular assembly spans both bacterial membranes and that of the infected host cell. The internal channel formed by the injectisome allows for the direct delivery of partially unfolded virulence effectors into the host cytoplasm(1). The structural foundation of the injectisome is the basal body, a molecular lock-nut structure composed predominantly of three proteins that form highly oligomerized concentric rings spanning the inner and outer membranes(2-5). Here we present the structure of the prototypical Salmonella enterica serovar Typhimurium pathogenicity island 1 basal body, determined using single-particle cryo-electron microscopy, with the inner-membrane-ring and outer-membranering oligomers defined at 4.3 angstrom and 3.6 angstrom resolution, respectively. This work presents the first, to our knowledge, high-resolution structural characterization of the major components of the basal body in the assembled state, including that of the widespread class of outer-membrane portals known as secretins.
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