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Article

Transition Pathway and Its Free-Energy Profile: A Protocol for Protein Folding Simulations

1
Korea Research Institute of Standards and Science, Daejon 305-340, Korea
2
School of Liberal Arts and Sciences, Korea National University of Transportation, Chungju 380-702, Korea
3
Center for In Silico Protein Science, School of Computational Sciences, Korea Institute for Advanced Study, Seoul 130-722, Korea
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2013, 14(8), 16058-16075; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms140816058
Received: 15 April 2013 / Revised: 22 July 2013 / Accepted: 29 July 2013 / Published: 2 August 2013
(This article belongs to the Collection Protein Folding)
We propose a protocol that provides a systematic definition of reaction coordinate and related free-energy profile as the function of temperature for the protein-folding simulation. First, using action-derived molecular dynamics (ADMD), we investigate the dynamic folding pathway model of a protein between a fixed extended conformation and a compact conformation. We choose the pathway model to be the reaction coordinate, and the folding and unfolding processes are characterized by the ADMD step index, in contrast to the common a priori reaction coordinate as used in conventional studies. Second, we calculate free-energy profile as the function of temperature, by employing the replica-exchange molecular dynamics (REMD) method. The current method provides efficient exploration of conformational space and proper characterization of protein folding/unfolding dynamics from/to an arbitrary extended conformation. We demonstrate that combination of the two simulation methods, ADMD and REMD, provides understanding on molecular conformational changes in proteins. The protocol is tested on a small protein, penta-peptide of met-enkephalin. For the neuropeptide met-enkephalin system, folded, extended, and intermediate sates are well-defined through the free-energy profile over the reaction coordinate. Results are consistent with those in the literature. View Full-Text
Keywords: molecular dynamics; free energy; reaction coordinate molecular dynamics; free energy; reaction coordinate
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MDPI and ACS Style

Lee, I.-H.; Kim, S.-Y.; Lee, J. Transition Pathway and Its Free-Energy Profile: A Protocol for Protein Folding Simulations. Int. J. Mol. Sci. 2013, 14, 16058-16075. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms140816058

AMA Style

Lee I-H, Kim S-Y, Lee J. Transition Pathway and Its Free-Energy Profile: A Protocol for Protein Folding Simulations. International Journal of Molecular Sciences. 2013; 14(8):16058-16075. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms140816058

Chicago/Turabian Style

Lee, In-Ho, Seung-Yeon Kim, and Jooyoung Lee. 2013. "Transition Pathway and Its Free-Energy Profile: A Protocol for Protein Folding Simulations" International Journal of Molecular Sciences 14, no. 8: 16058-16075. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms140816058

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