Page Stephani C, Silversmith Ruth E, Collins Edward J, Bourret Robert B
Department of Biochemistry & Biophysics, University of North Carolina , Chapel Hill, North Carolina 27599-7260, United States.
Department of Microbiology & Immunology, University of North Carolina , Chapel Hill, North Carolina 27599-7290, United States.
Biochemistry. 2015 Dec 15;54(49):7248-60. doi: 10.1021/acs.biochem.5b01082. Epub 2015 Dec 2.
In two-component signal transduction systems (TCSs), responses to stimuli are mediated through phosphotransfer between protein components. Canonical TCSs use His → Asp phosphotransfer in which phosphoryl groups are transferred from a conserved His on a sensory histidine kinase (HK) to a conserved Asp on a response regulator (RR). RRs contain the catalytic core of His → Asp phosphotransfer, evidenced by the ability of RRs to autophosphorylate with small molecule analogues of phospho-His proteins. Phosphorelays are a more complex variation of TCSs that additionally utilize Asp → His phosphotransfer through the use of an additional component, the histidine-containing phosphotransfer domain (Hpt), which reacts with RRs both as phosphodonors and phosphoacceptors. Here we show that imidazole has features of a rudimentary Hpt. Imidazole acted as a nucleophile and attacked phosphorylated RRs (RR-P) to produce monophosphoimidazole (MPI) and unphosphorylated RR. Phosphotransfer from RR-P to imidazole required the intact RR active site, indicating that the RR provided the core catalytic machinery for Asp → His phosphotransfer. Imidazole functioned in an artificial phosphorelay to transfer phosphoryl groups between unrelated RRs. The X-ray crystal structure of an activated RR·imidazole complex showed imidazole oriented in the RR active site similarly to the His of an Hpt. Imidazole interacted with RR nonconserved active site residues, which influenced the relative reactivity of RR-P with imidazole versus water. Rate constants for reaction of imidazole or MPI with chimeric RRs suggested that the RR active site contributes to the kinetic preferences exhibited by the YPD1 Hpt.
在双组分信号转导系统(TCSs)中,对刺激的反应是通过蛋白质组分之间的磷酸转移来介导的。典型的TCSs使用组氨酸→天冬氨酸的磷酸转移,其中磷酰基从传感组氨酸激酶(HK)上保守的组氨酸转移到反应调节因子(RR)上保守的天冬氨酸。RRs包含组氨酸→天冬氨酸磷酸转移的催化核心,这通过RRs与磷酸化组氨酸蛋白的小分子类似物进行自磷酸化的能力得到证明。磷酸中继是TCSs的一种更复杂的变体,它额外利用天冬氨酸→组氨酸的磷酸转移,通过使用一个额外的组分,即含组氨酸的磷酸转移结构域(Hpt),该结构域既作为磷供体又作为磷受体与RRs反应。在这里,我们表明咪唑具有原始Hpt的特征。咪唑作为亲核试剂攻击磷酸化的RRs(RR-P),产生单磷酸咪唑(MPI)和未磷酸化的RR。从RR-P到咪唑的磷酸转移需要完整的RR活性位点,这表明RR提供了天冬氨酸→组氨酸磷酸转移的核心催化机制。咪唑在人工磷酸中继中发挥作用,在不相关的RRs之间转移磷酰基。活化的RR·咪唑复合物的X射线晶体结构显示,咪唑在RR活性位点中的取向与Hpt的组氨酸类似。咪唑与RR非保守活性位点残基相互作用,这影响了RR-P与咪唑相对于水的相对反应性。咪唑或MPI与嵌合RRs反应的速率常数表明,RR活性位点有助于YPD1 Hpt表现出的动力学偏好。