Abstract

BackgroundDespite computational challenges, elucidating conformations that a protein system assumes under physiologic conditions for the purpose of biological activity is a central problem in computational structural biology. While these conformations are associated with low energies in the energy surface that underlies the protein conformational space, few existing conformational search algorithms focus on explicitly sampling low-energy local minima in the protein energy surface.MethodsThis work proposes a novel probabilistic search framework, PLOW, that explicitly samples low-energy local minima in the protein energy surface. The framework combines algorithmic ingredients from evolutionary computation and computational structural biology to effectively explore the subspace of local minima. A greedy local search maps a conformation sampled in conformational space to a nearby local minimum. A perturbation move jumps out of a local minimum to obtain a new starting conformation for the greedy local search. The process repeats in an iterative fashion, resulting in a trajectory-based exploration of the subspace of local minima.Results and conclusionsThe analysis of PLOW's performance shows that, by navigating only the subspace of local minima, PLOW is able to sample conformations near a protein's native structure, either more effectively or as well as state-of-the-art methods that focus on reproducing the native structure for a protein system. Analysis of the actual subspace of local minima shows that PLOW samples this subspace more effectively that a naive sampling approach. Additional theoretical analysis reveals that the perturbation function employed by PLOW is key to its ability to sample a diverse set of low-energy conformations. This analysis also suggests directions for further research and novel applications for the proposed framework.

Highlights

  • Despite computational challenges, elucidating conformations that a protein system assumes under physiologic conditions for the purpose of biological activity is a central problem in computational structural biology

  • Experiments conducted to study performance We conduct the following set of experiments to analyze the performance of the Protein Local Optima Walk (PLOW) framework: (I) Analysis of local minima: this first experiment explores the accuracy of the employed Associative Memory hamiltonian with Water (AMW) energy function with respect to local minima in order to determine the extent to which this energy function allows probing a selected true minimum in the protein energy surface. (II) Comparison of PLOW to the naive approach: this second experiment compares PLOW to the naive approach in sampling local minima, as described in the Methods section

  • PLOW essentially obtains a discrete representation of the relevant conformational space through a set of conformations that map to lowenergy local minima in the underlying protein energy surface

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Summary

Introduction

Despite computational challenges, elucidating conformations that a protein system assumes under physiologic conditions for the purpose of biological activity is a central problem in computational structural biology. Many experimental techniques, such as X-ray crystallography, nuclear magnetic resonance, and cryo-electron microscopy can elucidate one or a few structures populated under physiologic conditions. These techniques, cannot access the entire subspace of threedimensional arrangements ( referred to as conformations) that are available to the chain of amino acids in a protein molecule under physiologic conditions. Obtaining a representative view of the conformations available to a protein molecule under physiologic conditions presents an opportunity to improve our understanding of the structure-function relationship in proteins, and to advance the development of synthetically engineered proteins, improve our models of protein ligand docking for drug development, and assist in the prediction of protein-protein interactions in supramolecular assemblies [8,9,10]

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