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在Tad pilus系统电机CpaF中双向的柱子处理
Michael Hohl1, Emma J Banks2, Max P Manley1
1Department of Infectious Disease, Imperial College, London, UK.
Nature communications
|August 5, 2024
概括
细菌紧固粘附柱体系统 (TadPS) ATPase CpaF (TadA) 驱动柱体延伸和收缩. 这项研究揭示了CpaF.
科学领域:
- 微生物学 微生物学
- 结构生物学 结构生物学
- 生物化学 生物化学
背景情况:
- 细菌紧固粘附柱状系统 (TadPS) 对于病原体的粘附和殖民至关重要.
- 柱子的组装和动态是由ATPase CpaF (TadA) 驱动的,但它的机制仍然不清楚.
研究的目的:
- 阐明CpaF (TadA) 在驱动TadPS柱体动态中的分子机制.
- 描述CpaF的ATPase活性和形状变化的结构基础.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定不同核酸状态中的CpaF结构.
- 基于细胞的光显微镜来评估CpaF突变的体内功能.
- 生物化学试验用于研究核酸循环和形状变化.
主要成果:
- CpaF (TadA) 形成一个具有C2对称性的六合体,经历核酸依赖的构造变化.
- 核酸循环涉及一个子单元内部的状机制,驱动着连续的子单元变化.
- 突变分析确定了参与CpaF与平台蛋白相互作用的关键残留物 (CpaG/TadB,CpaH/TadC).
结论:
- 提出了一个CpaF (TadA) 驱动的双向柱状运动模型.
- 了解CpaF机制,可以了解更广泛的4型光纤组装ATPases家族.
- 这项工作对准人类病原体中的细菌粘附机制有影响.
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