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Unexpected Coelenterazine Degradation Products of Beroe abyssicola Photoprotein Photoinactivation.

Authors :
Burakova LP
Lyakhovich MS
Mineev KS
Petushkov VN
Zagitova RI
Tsarkova AS
Kovalchuk SI
Yampolsky IV
Vysotski ES
Kaskova ZM
Source :
Organic letters [Org Lett] 2021 Sep 03; Vol. 23 (17), pp. 6846-6849. Date of Electronic Publication: 2021 Aug 20.
Publication Year :
2021

Abstract

Ca <superscript>2+</superscript> -regulated photoproteins of ctenophores lose bioluminescence activity when exposed to visible light. Little is known about the chemical nature of chromophore photoinactivation. Using a total synthesis strategy, we have established the structures of two unusual coelenterazine products, isolated from recombinant berovin of the ctenophore Beroe abyssicola , which are Z / E isomers. We propose that during light irradiation, these derivatives are formed from 2-hydroperoxycoelenterazine via the intermediate 8a-peroxide by a mechanism reminiscent of that previously described for the auto-oxidation of green-fluorescent-protein-like chromophores.

Details

Language :
English
ISSN :
1523-7052
Volume :
23
Issue :
17
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
34416112
Full Text :
https://doi.org/10.1021/acs.orglett.1c02410