Coarse-grained free energy functions for studying protein conformational changes: A double-well network model

Jhih-Wei Chu, Gregory A. Voth*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

114 Scopus citations

Abstract

In this work, a double-well network model(DWNM)is presented for generating a coarse-grained free energy function that can be used to study the transition between reference conformational states of a protein molecule. Compared to earlier work that uses a single, multidimensional double-well potential to connect two conformational states, the DWNM uses a set of interconnected double-well potentials for this purpose. The DWNM free energy function has multiple intermediate states and saddle points, and is hence a "rough" free energy landscape. In this implementation of the DWNM, the free energy function is reduced to an elastic-network model representation near the two reference states. The effects of free energy function roughness on the reaction pathways of protein conformational change is demonstrated by applying theDWNMto the conformational changes of two protein systems: the coil-to-helix transition of the DB-loop in G-actin and the open-to-closed transition of adenylate kinase. In both systems, the rough free energy function of the DWNM leads to the identification of distinct minimum free energy paths connecting two conformational states. These results indicate that while the elastic-network model captures the low-frequency vibrational motions of a protein, the roughness in the free energy function introduced by theDWNMcan be used to characterize the transition mechanism between protein conformations.

Original languageEnglish
Pages (from-to)3860-3871
Number of pages12
JournalBiophysical Journal
Volume93
Issue number11
DOIs
StatePublished - 1 Dec 2007

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