DeepPath:利用基于物理的深度学习克服蛋白质转化途径预测的数据稀缺。

Yui Tik Pang, Katie M Kuo, Lixinhao Yang, James C Gumbart
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摘要

蛋白质的结构动力学在其功能中起着至关重要的作用,然而大多数实验和深度学习方法只产生静态模型。虽然分子动力学(MD)模拟提供了对构象转变的原子性洞察,但它们在计算上仍然是禁止的,特别是对于大规模的运动。在这里,我们介绍了DeepPath,这是一个基于深度学习的框架,可以在已知蛋白质状态之间快速生成物理上真实的过渡途径。与传统的监督学习方法不同,DeepPath采用主动学习来迭代地改进其预测,利用分子机械力场作为预言器来指导路径生成。我们在三个生物学相关的测试案例中验证了DeepPath: SHP2激活、CdiB H1分泌和BAM复合物侧门打开。DeepPath准确地预测了所有测试用例的转换路径,重现了之前研究中观察到的关键中间结构和瞬态相互作用。值得注意的是,DeepPath还预测了BAM向内和向外开放状态之间的中间状态,这与实验观察到的混合桶结构密切相关(TMscore = 0.91)。在所有情况下,DeepPath在数小时内实现了准确的途径预测,展示了一种有效的替代MD模拟来探索蛋白质构象转变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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DeepPath: Overcoming data scarcity for protein transition pathway prediction using physics-based deep learning.

The structural dynamics of proteins play a crucial role in their function, yet most experimental and deep learning methods produce only static models. While molecular dynamics (MD) simulations provide atomistic insight into conformational transitions, they remain computationally prohibitive, particularly for large-scale motions. Here, we introduce DeepPath, a deep-learning-based framework that rapidly generates physically realistic transition pathways between known protein states. Unlike conventional supervised learning approaches, DeepPath employs active learning to iteratively refine its predictions, leveraging molecular mechanical force fields as an oracle to guide pathway generation. We validated DeepPath on three biologically relevant test cases: SHP2 activation, CdiB H1 secretion, and the BAM complex lateral gate opening. DeepPath accurately predicted the transition pathways for all test cases, reproducing key intermediate structures and transient interactions observed in previous studies. Notably, DeepPath also predicted an intermediate between the BAM inward- and outward-open states that closely aligns with an experimentally observed hybrid-barrel structure (TMscore = 0.91). Across all cases, DeepPath achieved accurate pathway predictions within hours, showcasing an efficient alternative to MD simulations for exploring protein conformational transitions.

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