Chiu Christopher A, Stetson Sean, Thayer Kelly M
Quantitative Analysis CenterWesleyan University, Allbritton Center, 222 Church Street, Middletown, Connecticut 06459, United States.
Mathematics and Computer Science, Wesleyan University 54 Lawn Avenue, Hall-Atwater Laboratories, Chemistry Station, Middletown, Connecticut 06459, United States.
J Phys Chem B. 2025 Apr 17;129(15):3747-3760. doi: 10.1021/acs.jpcb.4c08495. Epub 2025 Apr 2.
Allosteric signaling in proteins allows perturbations at one locale to modulate activity at an orthosteric distant site. This may explain how distal mutations disrupt protein activity and offer pathways for the development of allosteric therapeutics, a novel class of restorative compounds to reactivate native function. Despite the ubiquitous presence of allosteric control in nature and the promises that it holds for treating currently untreatable diseases, quantitative theory of the mechanism of allostery is lacking. Working to fill this critical gap, we have developed a novel method to identify groups of covarying residues which the sector hypothesis suggests are capable of transmitting allosteric signals in proteins. A major problem with sectors computed from covariance measures is the selection relies upon a full covariance matrix rather than on the covariance among the residues posited to be in the sector. We demonstrate a novel method which constructs sectors on the basis of cohesion within the residues in the sector to eliminate the incongruity between the sector idea and the way it is calculated. Furthermore, the refinement can be iteratively applied, enabling the extraction of more than one sector in a well-defined, systematic manner. In this study, we report on the development of MD multi-sector selector and its application to allosteric signaling in the tumor suppressor protein p53. We consider the implications of our findings on our long-term goal of allosterically reactivating mutant p53 as a means of curing cancer, and critically assess the broader applicability of MD multi-sector selector across diverse fields.
蛋白质中的变构信号传导允许一个局部区域的扰动调节远位正构位点的活性。这或许可以解释远端突变如何破坏蛋白质活性,并为变构疗法的开发提供途径,变构疗法是一类新型的恢复性化合物,用于重新激活天然功能。尽管变构控制在自然界中普遍存在,且有望治疗目前无法治愈的疾病,但变构机制的定量理论仍很缺乏。为了填补这一关键空白,我们开发了一种新方法来识别共变残基组,扇形假说认为这些残基组能够在蛋白质中传递变构信号。从协方差度量计算得到的扇形的一个主要问题是,其选择依赖于完整的协方差矩阵,而不是假定在扇形中的残基之间的协方差。我们展示了一种新方法,该方法基于扇形内残基之间的凝聚性构建扇形,以消除扇形概念与其计算方式之间的不一致。此外,这种优化可以迭代应用,从而能够以明确、系统的方式提取多个扇形。在本研究中,我们报告了分子动力学多扇形选择器的开发及其在肿瘤抑制蛋白p53变构信号传导中的应用。我们考虑了我们的发现对我们将突变型p53变构激活作为治疗癌症手段的长期目标的影响,并严格评估了分子动力学多扇形选择器在不同领域的更广泛适用性。