The Photoactive Excited State of the B12-Based Photoreceptor CarH
Author(s) -
Nicholas A. Miller,
April K. Kaneshiro,
Arkaprabha Konar,
Roberto AlonsoMori,
Alexander Britz,
Aniruddha Deb,
James M. Glownia,
J. D. Koralek,
Leena Mallik,
Joseph H. Meadows,
Lindsay B. Michocki,
Tim B. van Driel,
Markos Koutmos,
S. Padmanabhan,
Montserrat ElíasArnanz,
Kevin J. Kubarych,
E. Neil G. Marsh,
James E. PennerHahn,
Roseanne J. Sension
Publication year - 2020
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.0c09428
Subject(s) - adenosylcobalamin , excited state , photochemistry , chemistry , homolysis , quantum yield , nanosecond , ultrafast laser spectroscopy , spectroscopy , fluorescence , atomic physics , optics , organic chemistry , radical , physics , laser , cofactor , quantum mechanics , enzyme
We have used transient absorption spectroscopy in the UV-visible and X-ray regions to characterize the excited state of CarH, a protein photoreceptor that uses a form of B 12 , adenosylcobalamin (AdoCbl), to sense light. With visible excitation, a nanosecond-lifetime photoactive excited state is formed with unit quantum yield. The time-resolved X-ray absorption near edge structure difference spectrum of this state demonstrates that the excited state of AdoCbl in CarH undergoes only modest structural expansion around the central cobalt, a behavior similar to that observed for methylcobalamin rather than for AdoCbl free in solution. We propose a new mechanism for CarH photoreactivity involving formation of a triplet excited state. This allows the sensor to operate with high quantum efficiency and without formation of potentially dangerous side products. By stabilizing the excited electronic state, CarH controls reactivity of AdoCbl and enables slow reactions that yield nonreactive products and bypass bond homolysis and reactive radical species formation.
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