Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536.
Microbial Sciences Institute, Yale University, West Haven, CT 06516.
Proc Natl Acad Sci U S A. 2022 Mar 15;119(11):e2117245119. doi: 10.1073/pnas.2117245119. Epub 2022 Mar 7.
SignificanceHow flagella sense complex environments and control bacterial motility remain fascinating questions. Here, we deploy cryo-electron tomography to determine in situ structures of the flagellar motor in wild-type and mutant cells of , revealing that three flagellar proteins (FliL, MotA, and MotB) form a unique supramolecular complex in situ. Importantly, FliL not only enhances motor function by forming a ring around the stator complex MotA/MotB in its extended, active conformation but also facilitates assembly of the stator complex around the motor. Our in situ data provide insights into how cooperative remodeling of the FliL-stator supramolecular complex helps regulate the collective ion flux and establishes the optimal function of the flagellar motor to guide bacterial motility in various environments.
意义
鞭毛如何感知复杂的环境并控制细菌的运动仍然是一个引人入胜的问题。在这里,我们利用低温电子断层扫描技术来确定野生型和突变型细胞中鞭毛马达的原位结构,揭示了三种鞭毛蛋白(FliL、MotA 和 MotB)在原位形成一个独特的超分子复合物。重要的是,FliL 不仅通过在其伸展的活性构象中形成围绕定子复合物 MotA/MotB 的环来增强马达功能,而且还促进定子复合物在马达周围的组装。我们的原位数据提供了关于 FliL-定子超分子复合物的协同重塑如何帮助调节集体离子通量的见解,并确立了鞭毛马达的最佳功能,以指导细菌在各种环境中的运动。