Dynamics and dissipation in enzyme catalysis.

Abstract:

:We use quantized molecular dynamics simulations to characterize the role of enzyme vibrations in facilitating dihydrofolate reductase hydride transfer. By sampling the full ensemble of reactive trajectories, we are able to quantify and distinguish between statistical and dynamical correlations in the enzyme motion. We demonstrate the existence of nonequilibrium dynamical coupling between protein residues and the hydride tunneling reaction, and we characterize the spatial and temporal extent of these dynamical effects. Unlike statistical correlations, which give rise to nanometer-scale coupling between distal protein residues and the intrinsic reaction, dynamical correlations vanish at distances beyond 4-6 Å from the transferring hydride. This work finds a minimal role for nonlocal vibrational dynamics in enzyme catalysis, and it supports a model in which nanometer-scale protein fluctuations statistically modulate--or gate--the barrier for the intrinsic reaction.

authors

Boekelheide N,Salomón-Ferrer R,Miller TF 3rd

doi

10.1073/pnas.1106397108

subject

Has Abstract

pub_date

2011-09-27 00:00:00

pages

16159-63

issue

39

eissn

0027-8424

issn

1091-6490

pii

1106397108

journal_volume

108

pub_type

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