AlphaMut: A Deep Reinforcement Learning Model to Suggest Helix-Disrupting Mutations.

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Chemical Theory and Computation Pub Date : 2025-01-14 Epub Date: 2024-12-19 DOI:10.1021/acs.jctc.4c01387
Prathith Bhargav, Arnab Mukherjee
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引用次数: 0

Abstract

Helices are important secondary structural motifs within proteins and are pivotal in numerous physiological processes. While amino acids (AA) such as alanine and leucine are known to promote helix formation, proline and glycine disfavor it. Helical structure formation, however, also depends on its environment, and hence, prior prediction of a mutational effect on a helical structure is difficult. Here, we employ a reinforcement learning algorithm to develop a predictive model for helix-disrupting mutations. We start with a model to disrupt helices independent of their protein environment. Our results show that only a few mutations lead to a drastic disruption of the target helix. We further extend our approach to helices in proteins and validate the results using rigorous free energy calculations. Our strategy identifies amino acids crucial for maintaining structural integrity and predicts key mutations that could alter protein structure. Through our work, we present a new use case for reinforcement learning in protein structure disruption.

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AlphaMut:一个深度强化学习模型来建议螺旋破坏突变。
螺旋是蛋白质中重要的二级结构基序,在许多生理过程中起着关键作用。众所周知,氨基酸(AA)如丙氨酸和亮氨酸能促进螺旋形成,而脯氨酸和甘氨酸则不利于螺旋形成。然而,螺旋结构的形成也取决于它的环境,因此,对螺旋结构的突变效应的预先预测是困难的。在这里,我们采用强化学习算法来开发螺旋破坏突变的预测模型。我们从一个独立于蛋白质环境破坏螺旋的模型开始。我们的结果表明,只有少数突变导致目标螺旋的剧烈破坏。我们进一步将我们的方法扩展到蛋白质中的螺旋,并使用严格的自由能计算验证结果。我们的策略确定了维持结构完整性至关重要的氨基酸,并预测了可能改变蛋白质结构的关键突变。通过我们的工作,我们提出了强化学习在蛋白质结构破坏中的新用例。
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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
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