Multiscale approach to the determination of the photoactive yellow protein signaling state ensemble

The nature of the optical cycle of photoactive yellow protein (PYP) makes its elucidation challenging for both experiment and theory. The long transition times render conventional simulation methods ineffective, and yet the short signaling-state lifetime makes experimental data difficult to obtain a...

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Published inPLoS computational biology Vol. 10; no. 10; p. e1003797
Main Authors A Rohrdanz, Mary, Zheng, Wenwei, Lambeth, Bradley, Vreede, Jocelyne, Clementi, Cecilia
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.10.2014
Public Library of Science (PLoS)
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Summary:The nature of the optical cycle of photoactive yellow protein (PYP) makes its elucidation challenging for both experiment and theory. The long transition times render conventional simulation methods ineffective, and yet the short signaling-state lifetime makes experimental data difficult to obtain and interpret. Here, through an innovative combination of computational methods, a prediction and analysis of the biological signaling state of PYP is presented. Coarse-grained modeling and locally scaled diffusion map are first used to obtain a rough bird's-eye view of the free energy landscape of photo-activated PYP. Then all-atom reconstruction, followed by an enhanced sampling scheme; diffusion map-directed-molecular dynamics are used to focus in on the signaling-state region of configuration space and obtain an ensemble of signaling state structures. To the best of our knowledge, this is the first time an all-atom reconstruction from a coarse grained model has been performed in a relatively unexplored region of molecular configuration space. We compare our signaling state prediction with previous computational and more recent experimental results, and the comparison is favorable, which validates the method presented. This approach provides additional insight to understand the PYP photo cycle, and can be applied to other systems for which more direct methods are impractical.
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Conceived and designed the experiments: MAR WZ CC. Performed the experiments: MAR WZ BL. Analyzed the data: MAR WZ CC. Contributed reagents/materials/analysis tools: JV. Wrote the paper: MAR CC.
Current address: The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America
Current address: NIDDK, NIH, Laboratory of Chemical Physics, Bethesda, Maryland, United States of America
Current address: Shell, Houston, Texas, United States of America
The authors have declared that no competing interests exist.
ISSN:1553-7358
1553-734X
1553-7358
DOI:10.1371/journal.pcbi.1003797