Unknown

Dataset Information

0

Short-Range Electron Transfer in Reduced Flavodoxin: Ultrafast Nonequilibrium Dynamics Coupled with Protein Fluctuations.


ABSTRACT: Short-range electron transfer (ET) in proteins is an ultrafast process on the similar time scales as local protein-solvent fluctuation, and thus the two dynamics are coupled. Here we use semiquinone flavodoxin and systematically characterized the photoinduced redox cycle with 11 mutations of different aromatic electron donors (tryptophan and tyrosine) and local residues to change redox properties. We observed the forward and backward ET dynamics in a few picoseconds, strongly following a stretched behavior resulting from a coupling between local environment relaxations and these ET processes. We further observed the hot vibrational-state formation through charge recombination and the subsequent cooling dynamics also in a few picoseconds. Combined with the ET studies in oxidized flavodoxin, these results coherently reveal the evolution of the ET dynamics from single to stretched exponential behaviors and thus elucidate critical time scales for the coupling. The observed hot vibration-state formation is robust and should be considered in all photoinduced back ET processes in flavoproteins.

SUBMITTER: Kundu M 

PROVIDER: S-EPMC7304529 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Short-Range Electron Transfer in Reduced Flavodoxin: Ultrafast Nonequilibrium Dynamics Coupled with Protein Fluctuations.

Kundu Mainak M   He Ting-Fang TF   Lu Yangyi Y   Wang Lijuan L   Zhong Dongping D  

The journal of physical chemistry letters 20180511 11


Short-range electron transfer (ET) in proteins is an ultrafast process on the similar time scales as local protein-solvent fluctuation, and thus the two dynamics are coupled. Here we use semiquinone flavodoxin and systematically characterized the photoinduced redox cycle with 11 mutations of different aromatic electron donors (tryptophan and tyrosine) and local residues to change redox properties. We observed the forward and backward ET dynamics in a few picoseconds, strongly following a stretch  ...[more]

Similar Datasets

| S-EPMC7272615 | biostudies-literature
| S-EPMC3909472 | biostudies-literature
| S-EPMC7258173 | biostudies-literature
| S-EPMC4970857 | biostudies-literature
| S-EPMC3449329 | biostudies-literature
| S-EPMC5572931 | biostudies-literature
| S-EPMC7367344 | biostudies-literature
| S-EPMC3593309 | biostudies-literature
| S-EPMC4903885 | biostudies-literature
| S-EPMC5938582 | biostudies-literature