| Literature DB >> 33174757 |
Nicholas A Miller1, April K Kaneshiro2, Arkaprabha Konar3, Roberto Alonso-Mori4, Alexander Britz4,5, Aniruddha Deb1,6, James M Glownia4, Jake D Koralek4, Leena Mallik1, Joseph H Meadows1, Lindsay B Michocki1, Tim B van Driel4, Markos Koutmos1,6, S Padmanabhan7, Montserrat Elías-Arnanz8, Kevin J Kubarych1, E Neil G Marsh1, James E Penner-Hahn1,6, Roseanne J Sension1,3,6.
Abstract
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 B12, 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.Entities:
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Year: 2020 PMID: 33174757 DOI: 10.1021/acs.jpcb.0c09428
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991