Identifying essential pairwise interactions in elastic network model using the alpha shape theory

Copyright © 2014 Wiley Periodicals, Inc.

Détails bibliographiques
Publié dans:Journal of computational chemistry. - 1984. - 35(2014), 15 vom: 05. Juni, Seite 1111-21
Auteur principal: Xia, Fei (Auteur)
Autres auteurs: Tong, Dudu, Yang, Lifeng, Wang, Dayong, Hoi, Steven C H, Koehl, Patrice, Lu, Lanyuan
Format: Article en ligne
Langue:English
Publié: 2014
Accès à la collection:Journal of computational chemistry
Sujets:Journal Article Research Support, Non-U.S. Gov't ANM ENM alpha shape theory elastic network model Proteins
Description
Résumé:Copyright © 2014 Wiley Periodicals, Inc.
Elastic network models (ENM) are based on the idea that the geometry of a protein structure provides enough information for computing its fluctuations around its equilibrium conformation. This geometry is represented as an elastic network (EN) that is, a network of links between residues. A spring is associated with each of these links. The normal modes of the protein are then identified with the normal modes of the corresponding network of springs. Standard approaches for generating ENs rely on a cutoff distance. There is no consensus on how to choose this cutoff. In this work, we propose instead to filter the set of all residue pairs in a protein using the concept of alpha shapes. The main alpha shape we considered is based on the Delaunay triangulation of the Cα positions; we referred to the corresponding EN as EN(∞). We have shown that heterogeneous anisotropic network models, called αHANMs, that are based on EN(∞) reproduce experimental B-factors very well, with correlation coefficients above 0.99 and root-mean-square deviations below 0.1 Å(2) for a large set of high resolution protein structures. The construction of EN(∞) is simple to implement and may be used automatically for generating ENs for all types of ENMs
Description:Date Completed 15.04.2015
Date Revised 28.04.2014
published: Print-Electronic
Citation Status MEDLINE
ISSN:1096-987X
DOI:10.1002/jcc.23587