Department of Chemistry, University of Kentucky, 505 Rose St., Chemistry-Physics Building, Lexington, KY, USA 40506.
Department of Molecular and Cellular Biochemistry, University of Kentucky, 741 South Limestone, St. Lexington, KY, USA 40536.
Biochim Biophys Acta Gen Subj. 2018 Dec;1862(12):2651-2659. doi: 10.1016/j.bbagen.2018.07.027. Epub 2018 Jul 31.
Calcineurin (CaN) is a serine/threonine phosphatase that regulates a variety of physiological and pathophysiological processes in mammalian tissue. The calcineurin (CaN) regulatory domain (RD) is responsible for regulating the enzyme's phosphatase activity, and is believed to be highly-disordered when inhibiting CaN, but undergoes a disorder-to-order transition upon diffusion-limited binding with the regulatory protein calmodulin (CaM). The prevalence of polar and charged amino acids in the regulatory domain (RD) suggests electrostatic interactions are involved in mediating calmodulin (CaM) binding, yet the lack of atomistic-resolution data for the bound complex has stymied efforts to probe how the RD sequence controls its conformational ensemble and long-range attractions contribute to target protein binding. In the present study, we investigated via computational modeling the extent to which electrostatics and structural disorder facilitate CaM/CaN association kinetics. Specifically, we examined several RD constructs that contain the CaM binding region (CAMBR) to characterize the roles of electrostatics versus conformational diversity in controlling diffusion-limited association rates, via microsecond-scale molecular dynamics (MD) and Brownian dynamic (BD) simulations. Our results indicate that the RD amino acid composition and sequence length influence both the dynamic availability of conformations amenable to CaM binding, as well as long-range electrostatic interactions to steer association. These findings provide intriguing insight into the interplay between conformational diversity and electrostatically-driven protein-protein association involving CaN, which are likely to extend to wide-ranging diffusion-limited processes regulated by intrinsically-disordered proteins.
钙调神经磷酸酶(CaN)是一种丝氨酸/苏氨酸磷酸酶,可调节哺乳动物组织中的多种生理和病理生理过程。钙调神经磷酸酶(CaN)调节结构域(RD)负责调节酶的磷酸酶活性,并且当抑制 CaN 时,被认为是高度无序的,但在与调节蛋白钙调蛋白(CaM)扩散限制结合时,会发生无序到有序的转变。调节结构域(RD)中极性和带电氨基酸的普遍性表明静电相互作用参与调节钙调蛋白(CaM)结合,但由于缺乏结合复合物的原子分辨率数据,阻碍了探测 RD 序列如何控制其构象集合以及长程吸引力如何有助于靶蛋白结合的努力。在本研究中,我们通过计算建模研究了静电和结构无序在多大程度上促进了 CaM/CaN 结合的动力学。具体而言,我们检查了几个包含 CaM 结合区域(CAMBR)的 RD 结构,以通过微秒级分子动力学(MD)和布朗动态(BD)模拟来表征静电与构象多样性在控制扩散限制结合速率中的作用。我们的结果表明,RD 氨基酸组成和序列长度会影响可与 CaM 结合的构象的动态可用性,以及长程静电相互作用以引导结合。这些发现为 CaN 涉及的构象多样性和静电驱动的蛋白质-蛋白质相互作用之间的相互作用提供了有趣的见解,这可能会扩展到广泛的由固有无序蛋白调节的扩散限制过程。