机器学习的自适应工作流程阐明了 TAK1 异构网络的顺序运行机制。

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemistry Biochemistry Pub Date : 2024-05-14 DOI:10.1021/acs.biochem.3c00643
Nibedita Ray Chaudhuri,  and , Shubhra Ghosh Dastidar*, 
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引用次数: 0

摘要

异构是驱动生物分子过程的基本机制,具有重要的治疗意义。我们的研究严格考察了两种不同的机器学习算法如何从构象集合混合物(从 2.4 μs 分子动力学(MD)模拟中获得)中对 TAK1 的两种已经接近活性的 DFG-in 状态进行独特的分类,这两种状态的区别仅仅在于是否存在异位激活剂 TAB1。然而,新颖之处在于了解更深层次的算法潜力,以系统性地推导出一系列不同的残基连接特征,从而重建 TAK1-TAB1 异构在这种接近活性的生化情景中的基本机理结构。基于随机森林的递归工作流程展示了对异构特征进行离散化、层次化推导的潜力,而基于多层感知器的方法在与互信息评分混合后,在揭示流体连接特征模式方面获得了相当大的功效。有趣的是,这两种方法都为 TAK1 激活的功能构象变化提供了相似的方向基准。这些发现突出了沿定向 C-lobe → 激活环 → ATP 袋信息流通道的关键激活特征,包括(1)αF-αE 位端排列和(2)激活环向激酶活性位点的 "催化 "漂移,从而大大推进了对机理的深入理解。此外,一些新的异构热点(K253、Y206、N189 等)被进一步确认为 TAB1 的传感器、换能器和反应器,包括一个基准 E70 突变位点,精确地绘制出了顺序异构执行的重要结构片段。因此,我们的工作展示了如何利用标准 ML 方法,在适应特定系统和目标的适当精简工作流程中,探索动态异构机制的更大结构深度和维度。
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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Adaptive Workflows of Machine Learning Illuminate the Sequential Operation Mechanism of the TAK1′s Allosteric Network

Allostery is a fundamental mechanism driving biomolecular processes that holds significant therapeutic concern. Our study rigorously investigates how two distinct machine-learning algorithms uniquely classify two already close-to-active DFG-in states of TAK1, differing just by the presence or absence of its allosteric activator TAB1, from an ensemble mixture of conformations (obtained from 2.4 μs molecular dynamics (MD) simulations). The novelty, however, lies in understanding the deeper algorithmic potentials to systematically derive a diverse set of differential residue connectivity features that reconstruct the essential mechanistic architecture for TAK1-TAB1 allostery in such a close-to-active biochemical scenario. While the recursive, random forest-based workflow displays the potential of conducting discretized, hierarchical derivation of allosteric features, a multilayer perceptron-based approach gains considerable efficacy in revealing fluid connected patterns of features when hybridized with mutual information scoring. Interestingly, both pipelines benchmark similar directions of functional conformational changes for TAK1′s activation. The findings significantly advance the depth of mechanistic understanding by highlighting crucial activation signatures along a directed C-lobe → activation loop → ATP pocket channel of information flow, including (1) the αF-αE biterminal alignments and (2) the “catalytic” drift of the activation loop toward kinase active site. Besides, some novel allosteric hotspots (K253, Y206, N189, etc.) are further recognized as TAB1 sensors, transducers, and responders, including a benchmark E70 mutation site, precisely mapping the important structural segments for sequential allosteric execution. Hence, our work demonstrates how to navigate through greater structural depths and dimensions of dynamic allosteric machineries just by leveraging standard ML methods in suitable streamlined workflows adaptive to the specific system and objectives.

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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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