接触后效应的蛋白质配体结合率的有限元估计:在肌钙蛋白C和SERCA中钙结合的应用。

P M Kekenes-Huskey, A Gillette, J Hake, J A McCammon
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引用次数: 19

摘要

我们介绍了一个计算管道和一套软件工具,用于根据最近发展的理论框架近似扩散限制绑定。我们的方法处理由高分辨率结构数据生成的分子几何形状,并可以解释隐藏在蛋白质内部或门控机制背后的活性位点。利用FEniCS库和APBS求解器的工具,我们为我们的方法实现了数字代码,并研究了两种Ca(2+)结合蛋白:肌钙蛋白C和肌浆网Ca(2+) atp酶(SERCA)。我们发现,扩散相遇和内部“埋藏通道”描述的组合提供了对关联率的优越描述,提高了数量级的估计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Finite Element Estimation of Protein-Ligand Association Rates with Post-Encounter Effects: Applications to Calcium binding in Troponin C and SERCA.

We introduce a computational pipeline and suite of software tools for the approximation of diffusion-limited binding based on a recently developed theoretical framework. Our approach handles molecular geometries generated from high-resolution structural data and can account for active sites buried within the protein or behind gating mechanisms. Using tools from the FEniCS library and the APBS solver, we implement a numerical code for our method and study two Ca(2+)-binding proteins: Troponin C and the Sarcoplasmic Reticulum Ca(2+) ATPase (SERCA). We find that a combination of diffusional encounter and internal 'buried channel' descriptions provide superior descriptions of association rates, improving estimates by orders of magnitude.

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