Immormino Robert M, Starbird Chrystal A, Silversmith Ruth E, Bourret Robert B
Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina 27599-7290, United States.
Biochemistry. 2015 Jun 9;54(22):3514-27. doi: 10.1021/acs.biochem.5b00286. Epub 2015 May 28.
Response regulator signaling proteins and phosphatases of the haloacid dehalogenase (HAD) superfamily share strikingly similar folds, active site geometries, and reaction chemistry. Proteins from both families catalyze the transfer of a phosphoryl group from a substrate to one of their own aspartyl residues, and subsequent hydrolysis of the phosphoprotein. Notable differences include an additional Asp that functions as an acid/base catalyst and an active site well-structured prior to phosphorylation in HAD phosphatases. Both features contribute to reactions substantially faster than those for response regulators. To investigate mechanisms underlying the functional differences between response regulators and HAD phosphatases, we characterized five double mutants of the response regulator CheY designed to mimic HAD phosphatases. Each mutant contained the extra Asp paired with a phosphatase-inspired substitution to potentially position the Asp properly. Only CheY DR (Arg as the anchor) exhibited enhanced rates of both autophosphorylation with phosphoramidate and autodephosphorylation compared to those of wild-type CheY. Crystal structures of CheY DR complexed with MoO4(2-) or WO4(2-) revealed active site hydrogen bonding networks similar to those in HAD·substrate complexes, with the extra Asp positioned for direct interaction with the leaving group (phosphorylation) or nucleophile (dephosphorylation). However, CheY DR reaction kinetics did not exhibit the pH sensitivities expected for acid/base catalysis. Biochemical analysis indicated CheY DR had an enhanced propensity to adopt the active conformation without phosphorylation, but a crystal structure revealed unphosphorylated CheY DR was not locked in the active conformation. Thus, the enhanced reactivity of CheY DR reflected partial acquisition of catalytic and structural features of HAD phosphatases.
卤代酸脱卤酶(HAD)超家族的响应调节信号蛋白和磷酸酶具有惊人相似的折叠结构、活性位点几何形状和反应化学性质。这两个家族的蛋白质都催化磷酰基从底物转移到自身的一个天冬氨酰残基上,随后催化磷蛋白的水解。显著的差异包括一个额外的天冬氨酸作为酸碱催化剂发挥作用,以及在HAD磷酸酶磷酸化之前活性位点结构良好。这两个特征都使得反应速度比响应调节蛋白的反应速度快得多。为了研究响应调节蛋白和HAD磷酸酶功能差异背后的机制,我们对响应调节蛋白CheY的五个双突变体进行了表征,这些突变体旨在模拟HAD磷酸酶。每个突变体都包含额外的天冬氨酸,并伴有一个受磷酸酶启发的取代基,以潜在地正确定位天冬氨酸。与野生型CheY相比,只有CheY DR(以精氨酸为锚定)表现出用氨基磷酸酯进行自磷酸化和自去磷酸化的速率都有所提高。与MoO4(2-) 或WO4(2-) 复合的CheY DR的晶体结构揭示了与HAD·底物复合物中相似的活性位点氢键网络,额外的天冬氨酸定位为与离去基团(磷酸化)或亲核试剂(去磷酸化)直接相互作用。然而,CheY DR反应动力学并未表现出酸碱催化预期的pH敏感性。生化分析表明,CheY DR在未磷酸化时更倾向于采用活性构象,但晶体结构显示未磷酸化的CheY DR并未锁定在活性构象中。因此,CheY DR反应活性的增强反映了对HAD磷酸酶催化和结构特征的部分获得。