Journal
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 14, Issue 47, Pages 10657-10663Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.3c02438
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This study provides a thorough investigation of the understanding of ultrafast short-range electron transfer in proteins, and conducts systematic studies on well-defined biological systems by utilizing two types of flavodoxins and designing mutants. The research identifies a position with a favorable orientation and distance for ultrafast electron transfer, and reveals that all forward and back electron transfer dynamics are ultrafast nonequilibrium processes.
The understanding of ultrafast short-range electron transfer (ET) in proteins remains challenging, and thorough studies on well-defined biological systems are demanding. Here, we utilized two types of flavodoxins and designed a series of mutants on two positions to systematically characterize the complete photoinduced redox cycles. We identified one position with a favorable orientation and distance for ultrafast ET in a few femtoseconds and the other position is relatively flexible with a longer ET time scale. We found that all forward and back ET dynamics are ultrafast nonequilibrium processes, occurring through highly vibronic states and ending in vibrationally hot ground states with subsequent cooling relaxation to efficiently dissipate photon energy into the protein environment.
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