Bacterial Transmembrane Systems Unit, Institut Pasteur, Université Paris Cité, CNRS UMR, Paris, France.
Structural Bioinformatics Unit, Institut Pasteur, Université Paris Cité, CNRS UMR, Paris, France.
Subcell Biochem. 2024;104:549-563. doi: 10.1007/978-3-031-58843-3_21.
Within the highly diverse type four filament (TFF or T4F) superfamily, the machineries of type IVa pili (T4aP) and the type 2 secretion system (T2SS) in diderm bacteria exhibit a substantial sequence similarity despite divergent functions and distinct appearances: T4aP can extend micrometers beyond the outer membrane, whereas the endopili in the T2SS are restricted to the periplasm. The determination of the structure of individual components and entire filaments is crucial to understand how their structure enables them to serve different functions. However, the dynamics of these filaments poses a challenge for their high-resolution structure determination. This review presents different approaches that have been used to study the structure and dynamics of T4aP and T2SS endopili by means of integrative structural biology, cryo-electron microscopy (cryo-EM), and molecular dynamics simulations. Their conserved features and differences are presented. The non-helical stretch in the long-conserved N-terminal helix which is characteristic of all members of the TFF and the impact of calcium on structure, function, and dynamics of these filaments are discussed in detail.
在高度多样化的四型纤维(TFF 或 T4F)超家族中,尽管功能不同,外观也不同,但 IVa 菌毛(T4aP)和 II 型分泌系统(T2SS)的机制在真细菌中表现出很大的序列相似性:T4aP 可以延伸到外膜之外数微米,而 T2SS 中的内菌毛则局限于周质。确定单个组件和整个纤维的结构对于了解它们的结构如何使它们能够发挥不同的功能至关重要。然而,这些纤维的动力学对其高分辨率结构的确定构成了挑战。本文综述了不同的方法,通过整合结构生物学、冷冻电子显微镜(cryo-EM)和分子动力学模拟,研究了 T4aP 和 T2SS 内菌毛的结构和动力学。介绍了它们的保守特征和差异。详细讨论了所有 TFF 成员所特有的长保守 N 端螺旋中非螺旋延伸以及钙对这些纤维结构、功能和动力学的影响。
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