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离子结合位点及其简化模型的表示。

Ion binding sites and their representations by reduced models.

机构信息

Department of Biochemistry and Molecular Biology, Gordon Center for Integrative Science, University of Chicago, Chicago, Illinois 60637, USA.

出版信息

J Phys Chem B. 2012 Jun 14;116(23):6966-79. doi: 10.1021/jp3007365. Epub 2012 Apr 30.

Abstract

The binding of small metal ions to complex macromolecular structures is typically dominated by strong local interactions of the ion with its nearest ligands. Progress in understanding the molecular determinants of ion selectivity can often be achieved by considering simplified reduced models comprised of only the most important ion-coordinating ligands. Although the main ingredients underlying simplified reduced models are intuitively clear, a formal statistical mechanical treatment is nonetheless necessary in order to draw meaningful conclusions about complex macromolecular systems. By construction, reduced models only treat the ion and the nearest coordinating ligands explicitly. The influence of the missing atoms from the protein or the solvent is incorporated indirectly. Quasi-chemical theory offers one example of how to carry out such a separation in the case of ion solvation in bulk liquids, and in several ways, a statistical mechanical formulation of reduced binding site models for macromolecules is expected to follow a similar route. However, there are also important differences when the ion-coordinating moieties are not solvent molecules from a bulk phase but are molecular ligands covalently bonded to a macromolecular structure. Here, a statistical mechanical formulation of reduced binding site models is elaborated to address these issues. The formulation provides a useful framework to construct reduced binding site models, and define the average effect from the surroundings on the ion and the nearest coordinating ligands.

摘要

小分子金属离子与复杂大分子结构的结合通常由离子与其最近配体的强局部相互作用主导。通过考虑仅由最重要的离子配位配体组成的简化还原模型,通常可以在理解离子选择性的分子决定因素方面取得进展。尽管简化还原模型的主要成分直观上很清楚,但为了对复杂的大分子系统得出有意义的结论,仍然需要进行正式的统计力学处理。通过构建,还原模型仅明确地处理离子和最近的配位配体。来自蛋白质或溶剂的缺失原子的影响是间接包含的。准化学理论提供了一种在体相液体中离子溶剂化的情况下如何进行这种分离的示例,并且在许多方面,大分子还原结合位点模型的统计力学公式化有望遵循类似的途径。然而,当配位部分不是来自体相的溶剂分子,而是共价键合到大分子结构上的分子配体时,也存在重要差异。在这里,阐述了一种简化结合位点模型的统计力学公式化方法来解决这些问题。该公式化方法为构建简化结合位点模型提供了有用的框架,并定义了周围环境对离子和最近配位配体的平均影响。

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