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不断发展的深度学习方法生态系统,用于建模蛋白质-蛋白质相互作用。

Growing ecosystem of deep learning methods for modeling protein-protein interactions.

机构信息

Department of Systems Biology, Columbia University, New York, NY 10032, USA.

出版信息

Protein Eng Des Sel. 2023 Jan 21;36. doi: 10.1093/protein/gzad023.

Abstract

Numerous cellular functions rely on protein-protein interactions. Efforts to comprehensively characterize them remain challenged however by the diversity of molecular recognition mechanisms employed within the proteome. Deep learning has emerged as a promising approach for tackling this problem by exploiting both experimental data and basic biophysical knowledge about protein interactions. Here, we review the growing ecosystem of deep learning methods for modeling protein interactions, highlighting the diversity of these biophysically informed models and their respective trade-offs. We discuss recent successes in using representation learning to capture complex features pertinent to predicting protein interactions and interaction sites, geometric deep learning to reason over protein structures and predict complex structures, and generative modeling to design de novo protein assemblies. We also outline some of the outstanding challenges and promising new directions. Opportunities abound to discover novel interactions, elucidate their physical mechanisms, and engineer binders to modulate their functions using deep learning and, ultimately, unravel how protein interactions orchestrate complex cellular behaviors.

摘要

许多细胞功能依赖于蛋白质-蛋白质相互作用。然而,由于蛋白质组中使用的分子识别机制的多样性,全面描述它们仍然具有挑战性。深度学习通过利用实验数据和关于蛋白质相互作用的基本生物物理知识,已成为解决这一问题的一种有前途的方法。在这里,我们回顾了用于建模蛋白质相互作用的深度学习方法不断发展的生态系统,强调了这些具有生物物理意义的模型的多样性及其各自的权衡。我们讨论了最近在使用表示学习来捕获与预测蛋白质相互作用和相互作用位点相关的复杂特征、几何深度学习来推理蛋白质结构和预测复杂结构以及生成式建模来设计全新的蛋白质组装方面的成功。我们还概述了一些突出的挑战和有前途的新方向。利用深度学习发现新的相互作用、阐明它们的物理机制以及设计结合物来调节它们的功能,最终揭示蛋白质相互作用如何协调复杂的细胞行为,这方面存在着大量的机会。

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