Jump to main content
Jump to site search

Issue 44, 2012
Previous Article Next Article

Water dynamics on the surface of the protein barstar

Author affiliations

Abstract

Water plays a fundamental function in life and technology. To gain a deeper knowledge to the problem of the hydration of biomolecules, the dynamics of water around an 89-residue protein of interest in molecular recognition, cancer cell research and amyloid fibrils investigations is analyzed. The biomolecule is the ribonuclease inhibitor barstar wild-type. The dynamics of the protein and the 7430 water molecules of the bath in which it is immersed is monitored during a period of 7 ns by using all-atom molecular dynamics simulations. The results confirm the existence of multiple time scales in the dynamics of water (10−1 to 103 ps) at the atomic level. That heterogeneity of residence times is not lost if the system of reference is just one atom of the inhibitor. The dehydration process of barstar is considered through the analysis of time correlation functions, obtaining an averaged decay time of τ = 84.0 ± 0.3 ps. A power law distribution, with scaling exponent α = 0.57 ± 0.04, suggests that this hydration water exhibits a scale free dynamics (with respect to the residence time of solvent molecules). Most of the water molecules located on the surface of the protein spend times smaller than the picosecond while only about 1% of them stay for periods of time on the nanosecond scale.

Graphical abstract: Water dynamics on the surface of the protein barstar

Back to tab navigation

Publication details

The article was received on 24 May 2012, accepted on 19 Sep 2012 and first published on 12 Oct 2012


Article type: Paper
DOI: 10.1039/C2CP41702B
Phys. Chem. Chem. Phys., 2012,14, 15393-15399

  •   Request permissions

    Water dynamics on the surface of the protein barstar

    M. C. Morón, Phys. Chem. Chem. Phys., 2012, 14, 15393
    DOI: 10.1039/C2CP41702B

Search articles by author

Spotlight

Advertisements