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Slow-Down in Diffusion in Crowded Protein Solutions Correlates with Transient Cluster Formation.
Nawrocki, Grzegorz; Wang, Po-Hung; Yu, Isseki; Sugita, Yuji; Feig, Michael.
Affiliation
  • Nawrocki G; Department of Biochemistry and Molecular Biology, Michigan State University , East Lansing, Michigan 48824, United States.
  • Wang PH; RIKEN Theoretical Molecular Science Laboratory , 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
  • Yu I; RIKEN Theoretical Molecular Science Laboratory , 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
  • Sugita Y; RIKEN iTHES , 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
  • Feig M; RIKEN Theoretical Molecular Science Laboratory , 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
J Phys Chem B ; 121(49): 11072-11084, 2017 12 14.
Article in En | MEDLINE | ID: mdl-29151345
ABSTRACT
For a long time, the effect of a crowded cellular environment on protein dynamics has been largely ignored. Recent experiments indicate that proteins diffuse more slowly in a living cell than in a diluted solution, and further studies suggest that the diffusion depends on the local surroundings. Here, detailed insight into how diffusion depends on protein-protein contacts is presented based on extensive all-atom molecular dynamics simulations of concentrated villin headpiece solutions. After force field adjustments in the form of increased protein-water interactions to reproduce experimental data, translational and rotational diffusion was analyzed in detail. Although internal protein dynamics remained largely unaltered, rotational diffusion was found to slow down more significantly than translational diffusion as the protein concentration increased. The decrease in diffusion is interpreted in terms of a transient formation of protein clusters. These clusters persist on sub-microsecond time scales and follow distributions that increasingly shift toward larger cluster size with increasing protein concentrations. Weighting diffusion coefficients estimated for different clusters extracted from the simulations with the distribution of clusters largely reproduces the overall observed diffusion rates, suggesting that transient cluster formation is a primary cause for a slow-down in diffusion upon crowding with other proteins.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Neurofilament Proteins / Molecular Dynamics Simulation Limits: Animals Language: En Journal: J Phys Chem B Journal subject: QUIMICA Year: 2017 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Neurofilament Proteins / Molecular Dynamics Simulation Limits: Animals Language: En Journal: J Phys Chem B Journal subject: QUIMICA Year: 2017 Document type: Article Affiliation country: United States