Searching for Structure: Characterizing the Protein Conformational Landscape with Clustering-Based Algorithms

聚类分析 二面角 拉马钱德兰地块 最大值和最小值 球状蛋白 层次聚类 蛋白质结构 算法 计算机科学 物理 结晶学 人工智能 化学 数学 分子 数学分析 氢键 核磁共振 量子力学
作者
Amanda C. Macke,Jacob E. Stump,Maria S. Kelly,Jamie Rowley,Vageesha Herath,Sarah Mullen,Ruxandra I. Dima
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
标识
DOI:10.1021/acs.jcim.3c01511
摘要

The identification and characterization of the main conformations from a protein population are a challenging and inherently high-dimensional problem. Here, we evaluate the performance of the Secondary sTructural Ensembles with machine LeArning (StELa) double-clustering method, which clusters protein structures based on the relationship between the φ and ψ dihedral angles in a protein backbone and the secondary structure of the protein, thus focusing on the local properties of protein structures. The classification of states as vectors composed of the clusters’ indices arising naturally from the Ramachandran plot is followed by the hierarchical clustering of the vectors to allow for the identification of the main features of the corresponding free energy landscape (FEL). We compare the performance of StELa with the established root-mean-squared-deviation (RMSD)-based clustering algorithm, which focuses on global properties of protein structures and with Combinatorial Averaged Transient Structure (CATS), the combinatorial averaged transient structure clustering method based on distributions of the φ and ψ dihedral angle coordinates. Using ensembles of conformations from molecular dynamics simulations of intrinsically disordered proteins (IDPs) of various lengths (tau protein fragments) or short fragments from a globular protein, we show that StELa is the clustering method that identifies many of the minima and relevant energy states around the minima from the corresponding FELs. In contrast, the RMSD-based algorithm yields a large number of clusters that usually cover most of the FEL, thus being unable to distinguish between states, while CATS does not sample well the FELs for long IDPs and fragments from globular proteins.

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