Miller Nicholas A, Kaneshiro April K, Konar Arkaprabha, Alonso-Mori Roberto, Britz Alexander, Deb Aniruddha, Glownia James M, Koralek Jake D, Mallik Leena, Meadows Joseph H, Michocki Lindsay B, van Driel Tim B, Koutmos Markos, Padmanabhan S, Elías-Arnanz Montserrat, Kubarych Kevin J, Marsh E Neil G, Penner-Hahn James E, Sension Roseanne J
Department of Chemistry, University of Michigan, 930 N University Ave. Ann Arbor, Michigan 48109-1055, United States.
Department of Biological Chemistry, University of Michigan, 1150 W. Medical Center Dr., Ann Arbor, Michigan 48109-0600, United States.
J Phys Chem B. 2020 Nov 25;124(47):10732-10738. doi: 10.1021/acs.jpcb.0c09428. Epub 2020 Nov 11.
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, 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.
我们利用紫外-可见和X射线区域的瞬态吸收光谱来表征CarH的激发态,CarH是一种蛋白质光感受器,它利用一种形式的B,腺苷钴胺素(AdoCbl)来感知光。在可见光激发下,形成了具有单位量子产率的纳秒寿命光活性激发态。该状态的时间分辨X射线吸收近边结构差谱表明,CarH中AdoCbl的激发态在中心钴周围仅发生适度的结构膨胀,这种行为类似于甲基钴胺素而非溶液中游离的AdoCbl所观察到的行为。我们提出了一种涉及三重态激发态形成的CarH光反应性新机制。这使得传感器能够以高量子效率运行,且不会形成潜在危险的副产物。通过稳定激发电子态,CarH控制AdoCbl的反应性,并实现产生非反应性产物的缓慢反应,绕过键的均裂和反应性自由基物种的形成。