Predicting receptor-ligand pairing preferences in plant-microbe interfaces via molecular dynamics and machine learning.

IF 4.1 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Computational and structural biotechnology journal Pub Date : 2025-06-18 eCollection Date: 2025-01-01 DOI:10.1016/j.csbj.2025.06.029
Erica T Prates, Omar Demerdash, Manesh Shah, Tomás A Rush, Udaya C Kalluri, Daniel A Jacobson
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引用次数: 0

Abstract

Microbiome assembly, structure, and dynamics significantly influence plant health. Secreted microbial signaling molecules initiate and mediate symbiosis by binding to structurally compatible plant receptors. For example, lipo-chitooligosaccharides (LCOs), produced by nitrogen-fixing rhizobial bacteria and various fungi, are recognized by plant lysin motif receptor-like kinases (LysM-RLKs), which activate the common symbiotic pathway. Accurately predicting these molecular interactions could reveal complementary signatures underlying the initial stages of endosymbiosis. Despite the breakthrough in protein-ligand structure prediction with deep learning-based tools, such as AlphaFold3, the large size and highly flexible nature of signaling compounds like LCOs present major challenges for detailed structural characterization and binding-affinity prediction. Typical structure-/physics-based methods of ligand virtual screening are designed for small, drug-like molecules, often rely on high-resolution, experimentally determined structures of the protein receptors, and rarely achieve sufficient sampling to obtain converged thermodynamic quantities with large ligands. In this study, we developed a hybrid molecular dynamics/machine learning (MD/ML) approach capable of predicting binding affinity rankings with high accuracy in systems involving large, flexible ligands, despite limited experimental structural information. Using coarse initial structural models, the predictions using the MD/ML workflow achieved strong alignment with experimental trends, particularly in the top-affinity tier for four legume LysM-RLKs (LYR3) binding to LCOs and a chitooligosaccharide. Furthermore, the MD-based conformation selection protocol provided critical structural insights into substrate specificity and binding mechanisms. This study demonstrates a powerful method to screen for challenging cognate ligand-receptors and advance our understanding of the molecular basis of microbial colonization in plants.

通过分子动力学和机器学习预测植物-微生物界面中的受体-配体配对偏好。
微生物组的组装、结构和动态显著影响植物健康。分泌的微生物信号分子通过与结构相容的植物受体结合来启动和介导共生。例如,由固氮根瘤菌和各种真菌产生的脂质壳寡糖(LCOs)可被植物溶酶基元受体样激酶(LysM-RLKs)识别,从而激活常见的共生途径。准确预测这些分子的相互作用可以揭示内在共生初始阶段的互补特征。尽管基于深度学习的工具(如AlphaFold3)在蛋白质配体结构预测方面取得了突破,但LCOs等信号化合物的大尺寸和高度灵活性为详细的结构表征和结合亲和力预测带来了重大挑战。典型的基于结构/物理的配体虚拟筛选方法是为小的药物样分子设计的,通常依赖于高分辨率的实验确定的蛋白质受体结构,并且很少实现足够的采样以获得大配体的收敛热力学量。在这项研究中,我们开发了一种混合分子动力学/机器学习(MD/ML)方法,能够在涉及大型柔性配体的系统中高精度地预测结合亲和力排名,尽管实验结构信息有限。使用粗糙的初始结构模型,使用MD/ML工作流的预测与实验趋势非常吻合,特别是在四种豆类LysM-RLKs (LYR3)与LCOs和壳寡糖结合的顶层亲和层。此外,基于md的构象选择方案提供了对底物特异性和结合机制的关键结构见解。该研究为筛选具有挑战性的同源配体受体提供了一种强有力的方法,并促进了我们对微生物在植物中定植的分子基础的理解。
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来源期刊
Computational and structural biotechnology journal
Computational and structural biotechnology journal Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
9.30
自引率
3.30%
发文量
540
审稿时长
6 weeks
期刊介绍: Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to: Structure and function of proteins, nucleic acids and other macromolecules Structure and function of multi-component complexes Protein folding, processing and degradation Enzymology Computational and structural studies of plant systems Microbial Informatics Genomics Proteomics Metabolomics Algorithms and Hypothesis in Bioinformatics Mathematical and Theoretical Biology Computational Chemistry and Drug Discovery Microscopy and Molecular Imaging Nanotechnology Systems and Synthetic Biology
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