Entropy connects water structure and dynamics in protein hydration layer

Click on the DOI link to access the article (may not be free). The enzyme Candida Antarctica lipase B (CALB) serves here as a model for understanding connections among hydration layer dynamics, solvation shell structure, and protein surface structure. The structure and dynamics of water molecules in...

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Bibliographic Details
Published in:Physical Chemistry Chemical Physics
Main Authors: Dahanayake, Jayangika Niroshani, Mitchell-Koch, Katie R.
Format: Article in Journal/Newspaper
Language:English
Published: Royal Society of Chemistry 2018
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Online Access:http://hdl.handle.net/10057/15363
https://doi.org/10.1039/c8cp01674g
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Summary:Click on the DOI link to access the article (may not be free). The enzyme Candida Antarctica lipase B (CALB) serves here as a model for understanding connections among hydration layer dynamics, solvation shell structure, and protein surface structure. The structure and dynamics of water molecules in the hydration layer were characterized for regions of the CALB surface, divided around each -helix, -sheet, and loop structure. Heterogeneous hydration dynamics were observed around the surface of the enzyme, in line with spectroscopic observations of other proteins. Regional differences in the structure of the biomolecular hydration layer were found to be concomitant with variations in dynamics. In particular, it was seen that regions of higher density exhibit faster water dynamics. This is analogous to the behavior of bulk water, where dynamics (diffusion coefficients) are connected to water structure (density and tetrahedrality) by excess (or pair) entropy, detailed in the Rosenfeld scaling relationship. Additionally, effects of protein surface topology and hydrophobicity on water structure and dynamics were evaluated using multiregression analysis, showing that topology has a somewhat larger effect on hydration layer structure-dynamics. Concave and hydrophobic protein surfaces favor a less dense and more tetrahedral solvation layer, akin to a more ice-like structure, with slower dynamics. Results show that pairwise entropies of local hydration layers, calculated from regional radial distribution functions, scale logarithmically with local hydration dynamics. Thus, the Rosenfeld relationship describes the heterogeneous structure-dynamics of the hydration layer around the enzyme CALB. These findings raise the question of whether this may be a general principle for understanding the structure-dynamics of biomolecular solvation. National Science Foundation under Grant No. CHE-1665157. This work is also supported by Wichita State University Department of Chemistry and Fairmount College of Liberal Arts and ...