结晶EM结构和结合表面排斥蛋白TraT的进化史
Chloe Seddon1,2, Sophia David3, Joshua L C Wong1
1Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Nature communications
|January 14, 2025
概括
抗菌素耐药性基因的传播受到细菌质粒上的TraT蛋白质的阻碍. 结构分析揭示了TraT的软木形状和膜定,这表明这种抵抗机制的独立进化.
科学领域:
- 微生物学 微生物学
- 结构生物学 结构生物学
- 遗传学 是一个遗传学.
背景情况:
- 结合是一种在细菌中传播抗微生物耐药性基因的关键机制.
- 类似IncF的等离子体利用TraS和TraT排除蛋白来防止同一等离子体的超级感染.
- 了解TraT的功能对于对抗抗生素耐药性至关重要.
研究的目的:
- 研究来自pKpQIL和F等离子体的TraT蛋白的结构和特异性.
- 探索TraT同类的进化起源和分布.
主要方法:
- 使用冷电子显微镜 (cryo-EM) 确定了TraTpKpQIL和TraTF的结构.
- 对来自等离子体和染色体的TraT序列进行了家族遗传学分析.
主要成果:
- TraTpKpQIL和TraTF形成了类似香瓶塞的十米结构.
- 这些结构通过经过修改的α-螺旋体管域固定在外膜上.
- 染色体TraT同类物在各种格兰阴性细菌中被确定,这表明其分布广泛.
- 在多个不同的进化系中发现了等离子体TraT序列,这表明了独立的获取事件.
结论:
- TraT 蛋白在等离子体表面排除中表现出特异性.
- 结构和遗传学数据表明,TraT在多个场合被不同的等离子体骨干独立地获得和选择.
- 这项研究提供了细菌结合和抗菌素耐药性传播的演变的见解.
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