中和抗体抑制p21H-ras分子开关的结构基础

William M. Gallagher , Guy H. Grant
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引用次数: 1

摘要

ras癌基因产物p21在参与细胞生长和分化的信号转导途径的早期阶段起着分子开关的作用。当蛋白质处于gtp络合形式时,它在信号转导中是活跃的,而在其gdp络合形式中是无活性的。p21ras的转化活性被小鼠单克隆抗体Y13-259中和,可能是通过阻止GDP-GTP交换。利用基于知识的预测方法和计算机辅助建模技术推导了Y13-259可变片段的分子模型。当与p21ras/(GDP)络合时,对该模型的分析表明,两个分子开关区域受到络合物形成的约束。抗体结合通过位阻机制抑制GDP-GTP交换。在确定了必要的抑制结合位点,并探索了它们的静电特性后,应该有可能继续设计抗体模拟物作为癌症控制的治疗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural basis of p21H-ras molecular switch inhibition by a neutralizing antibody

The ras oncogene product p21 functions as a molecular switch in the early section of the signal transduction pathway that is involved in cell growth and differentiation. When the protein is in its GTP-complexed form it is active in signal transduction, whereas it is inactive in its GDP-complexed form. The transforming activity of p21ras is neutralized by the mouse monoclonal antibody Y13-259, possibly by preventing GDP-GTP exchange. A molecular model of the variable fragment of Y13-259 has been derived using a knowledge-based prediction approach and computer-assisted modeling techniques. An analysis of this model while complexed with p21ras/(GDP) indicated that the two molecular switch regions are constrained by complex formation. Antibody binding inhibits GDP-GTP exchange through a mechanism of steric hindrance. Having identified necessary bound sites for inhibition, and explored their electrostatic properties, it should be possible to proceed with the design of antibody mimics as therapeutic agents in cancer control.

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