Thiol ester-linked p-coumaric acid as a new photoactive prosthetic group in a protein with rhodopsin-like photochemistry

W.D. Hoff, P. Dux, K. Hard, B. Devreese, I.M. Nugteren-Roodzant, W. Crielaard, R. Boelens, R. Kaptein, J. Van Beeumen, K.J. Hellingwerf

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A number of Eubacteria contain a photoactive yellow protein which has a photosensory function in negative phototaxis. It has been proposed that the cofactor responsible for the intense yellow color of this protein is retinal [McRee, D. E., et al. (1989) Proc. Natl. Acad. Sci. U.S.A. 86, 6533-6537]. This would make it the first eubacterial rhodopsin. Here we report the chemical structure of this chromophoric group to be p-coumaric acid, which is covalently bound to a unique cysteine in the apoprotein via a thiol ester bond, and thus not retinal. This makes PYP the first example of a protein containing p-coumaric acid, a metabolite previously found only in plants, as a prosthetic group and establishes the photoactive yellow proteins as a new type of photochemically active receptor molecule.
Original languageEnglish
Pages (from-to)13959-13962
Number of pages4
JournalBiochemistry
Volume33
Issue number47
DOIs
Publication statusPublished - 29 Jan 1994

Keywords

  • coumaric acid
  • rhodopsin
  • article
  • Eubacterium
  • nonhuman
  • photoreactivity
  • photoreceptor
  • priority journal
  • protein structure
  • structure analysis

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