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A New Approach for Investigating the Molecular Recognition of Protein: Toward Structure-Based Drug Design Based on the 3D-RISM Theory

机译:研究蛋白质分子识别的新方法:基于3D-RISM理论的基于结构的药物设计

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A new approach to investigate a molecular recognition process of protein is presented based on the three-dimensional reference interaction site model (3D-RISM) theory, a statistical mechanics theory of molecular liquids. Numerical procedure for solving the conventional 3D-RISM equation consists of two steps. In step 1, we solve ordinary RISM (or 1D-RISM) equations for a solvent mixture including target ligands in order to obtain the density pair correlation functions (PCF) among molecules in the solution. Then, we solve the 3D-RISM equation for a solute-solvent system to find three-dimensional density distribution functions (3D-DDF) of solvent species around a protein, using PCF obtained in the first step. A key to the success of the method was to regard a target Hgand as one of "solvent" species. However, the success is limited due to a difficulty of solving the 1D-RISM equation for a solvent mixture, including large ligand molecules. In the present paper, we propose a method which eases the limitation concerning solute size in the conventional method. In this approach, we solve a solute-solute 3D-RISM equations for a protein-ligand system in which both proteins and ligands are regarded as "solutes" at infinite dilution. The 3D- and 1D-RISM equations are solved for protein-solvent and ligand-solvent systems, respectively, in order to obtain the 3D- and 1D-DDF of solvent around the solutes, which are required for solving the solute-solute 3D-RISM equation. The method is applied to two practical and noteworthy examples concerning pharmaceutical design. One is an odorant binding protein in the Drosophila melanogaster, which binds an ethanol molecule. The other is phospholipase A2, which is known as a receptor of acetylsalicylic acid or aspirin. The result indicates that the method successfully reproduces the binding mode of the ligand molecules in the binding sites measured by the experiments.
机译:基于三维参考相互作用位点模型(3D-RISM)理论,一种分子液体的统计力学理论,提出了一种研究蛋白质分子识别过程的新方法。求解常规3D-RISM方程的数值过程包括两个步骤。在步骤1中,我们求解包含目标配体的溶剂混合物的常规RISM(或1D-RISM)方程,以获得溶液中分子之间的密度对相关函数(PCF)。然后,我们使用第一步中获得的PCF求解溶质溶剂系统的3D-RISM方程,以找到蛋白质周围溶剂物种的三维密度分布函数(3D-DDF)。该方法成功的关键是将目标配体视为“溶剂”物种之一。然而,由于难以求解包括大配体分子的溶剂混合物的1D-RISM方程,因此成功受到限制。在本文中,我们提出了一种减轻传统方法中溶质尺寸限制的方法。在这种方法中,我们求解蛋白质-配体系统的溶质-溶质3D-RISM方程,其中无限稀释的蛋白质和配体均被视为“溶质”。分别针对蛋白质-溶剂和配体-溶剂系统求解3D-和1D-RISM方程,以获得围绕溶质的溶剂的3D-和1D-DDF,这是解决溶质-溶质3D-所需的RISM方程。该方法被应用于有关药物设计的两个实用且值得注意的示例。一种是果蝇中的气味结合蛋白,它结合乙醇分子。另一个是磷脂酶A2,它被称为乙酰水杨酸或阿司匹林的受体。结果表明,该方法成功地再现了由实验测量的结合位点中的配体分子的结合模式。

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