细菌鞭毛体的方向切换的结构基础
Steven Johnson1, Justin C Deme2, Emily J Furlong3,4
1Center for Structural Biology, CCR, NCI, Frederick, MD, USA. steven.johnson2@nih.gov.
Nature microbiology
|March 8, 2024
概括
细菌的鞭毛旋转通过FliG蛋白的180°运动和MotA5B2定位器的转移来切换方向. 这种机制解释了离子流是如何推动细菌双向游泳的.
科学领域:
- 微生物学 微生物学
- 结构生物学 结构生物学
- 生物物理学的生物物理.
背景情况:
- 细菌鞭毛能够通过由离子流驱动的线丝旋转来实现运动.
- 了解旋转切换的机制对于细菌化学反应至关重要.
研究的目的:
- 阐明细菌鞭毛旋转切换的结构和机制基础.
- 为了可视化不同旋转状态中的鞭毛基底体和C环复合体.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定沙门氏菌鞭毛基底体的高分辨率结构.
- 对于反时钟方向和时钟方向的旋转形状,都获得了结构.
- 确定了MotA5B2定位器的高分辨率冷EM结构.
主要成果:
- 揭示了FliG蛋白的N端和C端域的180度构造变化.
- 在旋转逆转过程中,证明了MotA5B2定位器从C环的外部向内移动.
- 提供了原子层面的洞察力,了解稳定器和C环之间的相互作用.
结论:
- 定位器相对于C环的重新定位是切换鞭毛旋转方向的关键机制.
- 这个结构机制解释了单向的离子流如何转化为双向的鞭毛旋转.
- 这一发现有助于我们更好地了解细菌的运动性和能量转导.
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