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Communication: Capturing protein multiscale thermal fluctuations
Author(s) -
Kristopher Opron,
Kelin Xia,
Guo-Wei Wei
Publication year - 2015
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.4922045
Subject(s) - gaussian , statistical physics , scaling , cutoff , gaussian network model , computer science , flexibility (engineering) , set (abstract data type) , algorithm , biological system , linear scale , rigidity (electromagnetism) , macromolecule , thermal , physics , mathematics , chemistry , statistics , geometry , thermodynamics , biology , biochemistry , geodesy , quantum mechanics , programming language , geography
Existing elastic network models are typically parametrized at a given cutoff distance and often fail to properly predict the thermal fluctuation of many macromolecules that involve multiple characteristic length scales. We introduce a multiscale flexibility-rigidity index (mFRI) method to resolve this problem. The proposed mFRI utilizes two or three correlation kernels parametrized at different length scales to capture protein interactions at corresponding scales. It is about 20% more accurate than the Gaussian network model (GNM) in the B-factor prediction of a set of 364 proteins. Additionally, the present method is able to deliver accurate predictions for some large macromolecules on which GNM fails to produce accurate predictions. Finally, for a protein of N residues, mFRI is of linear scaling (O(N)) in computational complexity, in contrast to the order of O(N(3)) for GNM.

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