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钙调蛋白与钙离子结合后的构象可塑性为其与炭疽芽孢杆菌水肿因子的相互作用提供了一个模型。

The conformational plasticity of calmodulin upon calcium complexation gives a model of its interaction with the oedema factor of Bacillus anthracis.

作者信息

Laine Elodie, Yoneda Julliane D, Blondel Arnaud, Malliavin Thérèse E

机构信息

Unité de Bioinformatique Structurale, CNRS URA 2185 Institut Pasteur, 25-28, rue du Dr. Roux, Paris 75 724, France.

出版信息

Proteins. 2008 Jun;71(4):1813-29. doi: 10.1002/prot.21862.

Abstract

We analyzed the conformational plasticity of calmodulin (CaM) when it is bound to the oedema factor (EF) of Bacillus anthracis and its response to calcium complexation with molecular dynamics (MD) simulations. The EF-CaM complex was simulated during 15 ns for three different levels of calcium bound to CaM. They were respectively no calcium ion (EF-(Apo-CaM)), two calcium ions bound to the C-terminal domain of CaM (EF-(2Ca-CaM)), and four calcium ions bound to CaM (EF-(4Ca-CaM)). Calculations were performed using AMBER package. The analysis of the MD simulations illustrates how CaM forces EF in an open conformation to form the adenylyl cyclase enzymatic site, especially with the two calcium form of CaM, best suited to fit the open conformation of EF. By contrast, CaM encounters bending and unwinding of its flexible interlinker in EF-(Apo-CaM) and EF-(4Ca-CaM). Calcium binding to one domain of CaM affects the other one, showing a transmission of information along the protein structure. The analysis of the CaM domains conformation along the simulations brings an atomistic and dynamic explanation for the instability of these complexes. Indeed the EF-hand helices of the N-terminal domain tend to open upon calcium binding (EF-(4Ca-CaM)), although the domain is locked by EF. By contrast, the C-terminal domain is strongly locked in the open conformation by EF, and the removal of calcium induces a collapse of EF catalytic site (EF-(Apo-CaM)).

摘要

我们通过分子动力学(MD)模拟分析了钙调蛋白(CaM)与炭疽芽孢杆菌水肿因子(EF)结合时的构象可塑性及其对钙络合的响应。针对与CaM结合的三种不同钙水平,对EF-CaM复合物进行了15纳秒的模拟。它们分别是无钙离子(EF-(Apo-CaM))、两个钙离子结合到CaM的C末端结构域(EF-(2Ca-CaM))以及四个钙离子结合到CaM(EF-(4Ca-CaM))。使用AMBER软件包进行计算。MD模拟分析表明,CaM如何迫使EF处于开放构象以形成腺苷酸环化酶酶活性位点,特别是对于CaM的两个钙离子形式,最适合于适应EF的开放构象。相比之下,在EF-(Apo-CaM)和EF-(4Ca-CaM)中,CaM的柔性连接体出现弯曲和解开。钙离子与CaM的一个结构域结合会影响另一个结构域,显示出沿蛋白质结构的信息传递。沿着模拟对CaM结构域构象的分析为这些复合物的不稳定性提供了原子水平和动态的解释。实际上,N末端结构域的EF手型螺旋在结合钙离子时倾向于打开(EF-(4Ca-CaM)),尽管该结构域被EF锁定。相比之下,C末端结构域被EF强烈锁定在开放构象中,去除钙离子会导致EF催化位点塌陷(EF-(Apo-CaM))。

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