在Salmonella感染期间,宿主细胞活性细胞骨的颠覆结构的基础
Biao Yuan1,2,3, Jonas Scholz4, Jiri Wald1,2,3
1University Medical Center Hamburg-Eppendorf (UKE), Institute of Structural and Systems Biology, Hamburg, Germany.
Science advances
|December 8, 2023
概括
沙门氏菌使用III型分泌系统 (T3SS) 蛋白质Sipa和SipC来感染宿主细胞. 这项研究揭示了SipA如何稳定活性丝,SipC如何增强SipA.
科学领域:
- 微生物学 微生物学
- 细胞生物学 细胞生物学
- 结构生物学 结构生物学
背景情况:
- 分泌的细菌III型分泌系统 (T3SS) 蛋白质对于病原体感染至关重要.
- 沙门氏菌Sipa和SipC蛋白在感染期间颠覆宿主细胞细胞骨架,但它们的相互作用尚不清楚.
研究的目的:
- 为了阐明在宿主细胞入侵期间沙门氏菌SipA和SipC之间的分子相互作用.
- 了解通过SipA和SipC稳定F-actin的机制.
主要方法:
- 使用冷电子显微镜来确定与F-actin结合的Sipa的结构.
- 生物化学试验被用来分析Sipa,SipC和F-actin之间的相互作用.
主要成果:
- SipA以独特的模式与F-actin沟结合,稳定了丝.
- SipA通过关闭F-actin ATP口袋来防止无机酸盐从ATP释放.
- SipC增强了Sipa与F-actin的结合,这表明了一种连续感染机制.
结论:
- 该研究揭示了T3SS蛋白质Sipa和SipC在沙门氏菌感染中的协调作用.
- 了解这种机制为制定干扰沙门氏菌因子的策略提供了基础.
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