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.
journal_name
Proc Natl Acad Sci U S Aauthors
Boekelheide N,Salomón-Ferrer R,Miller TF 3rddoi
10.1073/pnas.1106397108subject
Has Abstractpub_date
2011-09-27 00:00:00pages
16159-63issue
39eissn
0027-8424issn
1091-6490pii
1106397108journal_volume
108pub_type
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