由可转移的机器学习模型生成的蛋白质侧链反映射重权重配置†

IF 3.2 3区 工程技术 Q2 CHEMISTRY, PHYSICAL
Jacob I. Monroe
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引用次数: 0

摘要

多尺度建模需要将不同细节级别的模型连接起来,其目标是从较低保真度的模型中获得加速度,同时从较高分辨率的模型中恢复精细细节。跨分辨率的通信在软物质建模中尤为重要,其中分子级细节和中尺度结构之间存在紧密耦合。虽然生物分子的多尺度建模已成为探索其结构和自组装的关键组成部分,但尽管最近通过机器学习取得了进展,但从粗粒度到细粒度或原子的反向映射表示仍然存在挑战。一个主要的障碍,特别是对于利用机器学习的策略,是反向映射只能近似地恢复感兴趣的原子集合。我们证明了反向映射配置可以重新加权以精确恢复所需原子集成的条件。通过训练每个侧链类型的单独解码模型,我们开发了一种基于归一化流和几何代数注意的算法,可以自回归地提出任何蛋白质序列的反向映射配置。对于现代蛋白质力场的重加权至关重要,我们训练的模型包括反向映射中的所有氢原子,并使与原子配置相关的概率直接可访问。然而,我们也证明,尽管最近开发的指标和原子蛋白质力场中低能量配置的生成具有最先进的性能,但重新加权是极具挑战性的。通过对构型权值的详细分析,我们表明机器学习的反向映射不仅要生成具有合理能量的构型,而且要在生成模型下正确分配相对概率。在原子分子构型的生成建模中,这些是非常重要的考虑因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reweighting configurations generated by transferable, machine learned models for protein sidechain backmapping†

Reweighting configurations generated by transferable, machine learned models for protein sidechain backmapping†

Multiscale modeling requires the linking of models at different levels of detail, with the goal of gaining accelerations from lower fidelity models while recovering fine details from higher resolution models. Communication across resolutions is particularly important in modeling soft matter, where tight couplings exist between molecular-level details and mesoscale structures. While multiscale modeling of biomolecules has become a critical component in exploring their structure and self-assembly, backmapping from coarse-grained to fine-grained, or atomistic, representations presents a challenge, despite recent advances through machine learning. A major hurdle, especially for strategies utilizing machine learning, is that backmappings can only approximately recover the atomistic ensemble of interest. We demonstrate conditions for which backmapped configurations may be reweighted to exactly recover the desired atomistic ensemble. By training separate decoding models for each sidechain type, we develop an algorithm based on normalizing flows and geometric algebra attention to autoregressively propose backmapped configurations for any protein sequence. Critical for reweighting with modern protein force fields, our trained models include all hydrogen atoms in the backmapping and make probabilities associated with atomistic configurations directly accessible. We also demonstrate, however, that reweighting is extremely challenging despite state-of-the-art performance on recently developed metrics and generation of configurations with low energies in atomistic protein force fields. Through detailed analysis of configurational weights, we show that machine-learned backmappings must not only generate configurations with reasonable energies, but also correctly assign relative probabilities under the generative model. These are broadly important considerations in generative modeling of atomistic molecular configurations.

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来源期刊
Molecular Systems Design & Engineering
Molecular Systems Design & Engineering Engineering-Biomedical Engineering
CiteScore
6.40
自引率
2.80%
发文量
144
期刊介绍: Molecular Systems Design & Engineering provides a hub for cutting-edge research into how understanding of molecular properties, behaviour and interactions can be used to design and assemble better materials, systems, and processes to achieve specific functions. These may have applications of technological significance and help address global challenges.
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