Biology Department, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112, United States.
J Mol Biol. 2018 Mar 30;430(7):1051-1064. doi: 10.1016/j.jmb.2018.02.004. Epub 2018 Feb 14.
In Escherichia coli chemosensory arrays, transmembrane receptors, a histidine autokinase CheA, and a scaffolding protein CheW interact to form an extended hexagonal lattice of signaling complexes. One interaction, previously assigned a crucial signaling role, occurs between chemoreceptors and the CheW-binding P5 domain of CheA. Structural studies showed a receptor helix fitting into a hydrophobic cleft at the boundary between P5 subdomains. Our work aimed to elucidate the in vivo roles of the receptor-P5 interface, employing as a model the interaction between E. coli CheA and Tsr, the serine chemoreceptor. Crosslinking assays confirmed P5 and Tsr contacts in vivo and their strict dependence on CheW. Moreover, the P5 domain only mediated CheA recruitment to polar receptor clusters if CheW was also present. Amino acid replacements at CheA.P5 cleft residues reduced CheA kinase activity, lowered serine response cooperativity, and partially impaired chemotaxis. Pseudoreversion studies identified suppressors of P5 cleft defects at other P5 groove residues or at surface-exposed residues in P5 subdomain 1, which interacts with CheW in signaling complexes. Our results indicate that a high-affinity P5-receptor binding interaction is not essential for core complex function. Rather, P5 groove residues are probably required for proper cleft structure and/or dynamic behavior, which likely impact conformational communication between P5 subdomains and the strong binding interaction with CheW that is necessary for kinase activation. We propose a model for signal transmission in chemotaxis signaling complexes in which the CheW-receptor interface plays the key role in conveying signaling-related conformational changes from receptors to the CheA kinase.
在大肠杆菌化学感觉阵列中,跨膜受体、组氨酸自动激酶 CheA 和支架蛋白 CheW 相互作用,形成信号复合物的扩展六边形晶格。先前被赋予关键信号作用的一种相互作用发生在化学感受器和 CheA 的 CheW 结合 P5 结构域之间。结构研究表明,受体螺旋适合于 P5 亚结构域之间边界的疏水区隙。我们的工作旨在阐明受体-P5 界面的体内作用,以大肠杆菌 CheA 和丝氨酸化学感受器 Tsr 之间的相互作用作为模型。交联测定证实了 P5 和 Tsr 在体内的相互作用及其对 CheW 的严格依赖性。此外,只有当 CheW 也存在时,P5 结构域才能介导 CheA 募集到极性受体簇。CheA.P5 裂缝残基的氨基酸替换降低了 CheA 激酶活性,降低了丝氨酸响应协同性,并部分损害了趋化性。假回复研究确定了其他 P5 沟槽残基或 P5 亚结构域 1 表面暴露残基处的 P5 裂缝缺陷的抑制因子,这些残基在信号复合物中与 CheW 相互作用。我们的结果表明,高亲和力的 P5-受体结合相互作用对于核心复合物功能不是必需的。相反,P5 沟槽残基可能对于适当的裂缝结构和/或动态行为是必需的,这可能影响 P5 亚结构域之间的构象通讯以及与 CheW 的强结合相互作用,这对于激酶激活是必需的。我们提出了一个在趋化信号复合物中信号转导的模型,其中 CheW-受体界面在将与信号相关的构象变化从受体传递到 CheA 激酶中起着关键作用。