Pang Yui Tik, Kuo Katie M, Yang Lixinhao, Gumbart James C
School of Physics, Georgia Institute of Technology, Atlanta, GA 30332, USA.
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA.
bioRxiv. 2025 Mar 2:2025.02.27.640693. doi: 10.1101/2025.02.27.640693.
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.
蛋白质的结构动力学在其功能中起着至关重要的作用,但大多数实验方法和深度学习方法仅生成静态模型。虽然分子动力学(MD)模拟能提供关于构象转变的原子层面见解,但计算成本仍然过高,尤其是对于大规模运动。在此,我们引入了DeepPath,这是一个基于深度学习的框架,可快速生成已知蛋白质状态之间符合物理现实的转变途径。与传统的监督学习方法不同,DeepPath采用主动学习来迭代优化其预测,利用分子力学力场作为“预言机”来指导途径生成。我们在三个生物学相关的测试案例上验证了DeepPath:SHP2激活、CdiB H1分泌以及BAM复合物侧向门打开。DeepPath准确预测了所有测试案例的转变途径,重现了先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一个中间体,该中间体与实验观察到的混合桶状结构紧密对齐(TMscore = 0.91)。在所有案例中,DeepPath在数小时内实现了准确的途径预测,展示了一种高效的替代MD模拟的方法,用于探索蛋白质构象转变。