Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66047, United States.
Protein Structure Laboratory, Del Shankel Structural Biology Center, University of Kansas, Lawrence, KS 66047, United States.
J Mol Biol. 2020 Dec 4;432(24):166693. doi: 10.1016/j.jmb.2020.10.027. Epub 2020 Oct 27.
Many Gram-negative bacterial pathogens use type III secretion systems (T3SS) to inject proteins into eukaryotic cells to subvert normal cellular functions. The T3SS apparatus (injectisome) shares a common architecture in all systems studied thus far, comprising three major components - the cytoplasmic sorting platform, envelope-spanning basal body and external needle with tip complex. The sorting platform consists of an ATPase (SctN) connected to "pods" (SctQ) having six-fold symmetry via radial spokes (SctL). These pods interface with the 24-fold symmetric SctD inner membrane ring (IR) via an adaptor protein (SctK). Here we report the first high-resolution structure of a SctK protein family member, PscK from Pseudomonas aeruginosa, as well as the structure of its interacting partner, the cytoplasmic domain of PscD (SctD). The cytoplasmic domain of PscD forms a forkhead-associated (FHA) fold, like that of its homologues from other T3SS. PscK, on the other hand, forms a helix-rich structure that does not resemble any known protein fold. Based on these structural findings, we present the first model for an interaction between proteins from the sorting platform and the IR. We also test the importance of the PscD residues predicted to mediate this electrostatic interaction using a two-hybrid analysis. The functional need for these residues in vivo was then confirmed by monitoring secretion of the effector ExoU. These structures will contribute to the development of atomic-resolution models of the entire sorting platform and to our understanding of the mechanistic interface between the sorting platform and the basal body of the injectisome.
许多革兰氏阴性细菌病原体使用 III 型分泌系统 (T3SS) 将蛋白质注入真核细胞,以颠覆正常的细胞功能。迄今为止研究的所有系统中,T3SS 装置(注入器)都具有共同的结构,由三个主要组件组成 - 细胞质分拣平台、包膜跨越基底体和带有尖端复合物的外部针。分拣平台由与通过辐射状辐条(SctL)连接的六重对称“荚”(SctQ)的 ATP 酶(SctN)组成。这些荚通过衔接蛋白(SctK)与 24 重对称 SctD 内膜环(IR)相互作用。在这里,我们报告了第一个 SctK 蛋白家族成员 Pseudomonas aeruginosa 中的 PscK 的高分辨率结构,以及其相互作用伙伴 PscD(SctD)的细胞质结构域的结构。PscD 的细胞质结构域形成了一个与其他 T3SS 同源物类似的叉头相关 (FHA) 折叠。另一方面,PscK 形成一个富含螺旋的结构,与任何已知的蛋白质折叠都不相似。基于这些结构发现,我们提出了第一个分拣平台和 IR 之间蛋白质相互作用的模型。我们还使用双杂交分析测试了预测介导这种静电相互作用的 PscD 残基的重要性。然后通过监测效应物 ExoU 的分泌来确认这些残基在体内的功能需求。这些结构将有助于开发整个分拣平台的原子分辨率模型,并加深我们对分拣平台和注入器基底体之间的机械界面的理解。