Bioluminescence of a number of marine organisms is conditioned by Ca-regulated photoprotein (CaRP) with coelenterazine as the reaction substrate. The reaction product, coelenteramide, at the first singlet excited state (S) is the emitter of CaRP. The S-state coelenteramide is produced via the decomposition of coelenterazine dioxetanone. Experiments suggested that the neutral S-coelenteramide is the primary emitter species. This supposition contradicts with theoretical calculations showing that the anionic S-coelenteramide is a primary product of the decomposition of coelenterazine dioxetanone. In this study, applying molecular dynamic (MD) simulations and the hybrid quantum mechanics/molecular mechanics (QM/MM) method, we investigated a proton-transfer (PT) process taking place in CaRP obelin from for emitter formation. Our calculations demonstrate a concerted PT process with a water molecule as a bridge between anionic S-coelenteramide and the nearest histidine residue. The low activation barrier as well as the strong hydrogen-bond network between the proton donor and the proton acceptor suggests a fast PT process comparable with that of the lifetime of excited anionic S-coelenteramide. The existence of the PT process eliminates the discrepancy between experimental and theoretical studies. The fast PT process at emitter formation can also take place in other CaRPs.
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http://dx.doi.org/10.1021/acs.jpcb.1c03985 | DOI Listing |
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