zFP538, a Yellow-Fluorescent Protein from Zoanthus, Contains a Novel Three-Ring Chromophore

Crystal structures of the tetrameric yellow-fluorescent protein zFP538 from the button polyp Zoanthus sp. and a green-emitting mutant (K66M) are presented. The atomic models have been refined at 2.7 and 2.5 Å resolution, with final crystallographic R factors of 0.206 (R free = 0.255) and 0.190 (R fr...

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Published in:Biochemistry (Easton) Vol. 44; no. 1; pp. 202 - 212
Main Authors: Remington, S. James, Wachter, Rebekka M, Yarbrough, Daniel K, Branchaud, Bruce, Anderson, D. C, Kallio, Karen, Lukyanov, Konstantin A
Format: Journal Article
Language:English
Published: United States American Chemical Society 11-01-2005
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Summary:Crystal structures of the tetrameric yellow-fluorescent protein zFP538 from the button polyp Zoanthus sp. and a green-emitting mutant (K66M) are presented. The atomic models have been refined at 2.7 and 2.5 Å resolution, with final crystallographic R factors of 0.206 (R free = 0.255) and 0.190 (R free = 0.295), respectively, and have excellent stereochemistry. The fold of the protomer is very similar to that of green (GFP) and red (DsRed) fluorescent proteins; however, evidence from crystallography and mass spectrometry suggests that zFP538 contains a three-ring chromophore derived from that of GFP. The yellow-emitting species (λem max = 538 nm) is proposed to result from a transimination reaction in which a transiently appearing DsRed-like acylimine is attacked by the terminal amino group of lysine 66 to form a new six-membered ring, cleaving the polypeptide backbone at the 65−66 position. This extends the chromophore conjugation by an additional double bond compared to GFP, lowering the absorption and emission frequencies. Substitution of lysine 66 with aspartate or glutamate partially converts zFP538 into a red-fluorescent protein, providing additional support for an acylimine intermediate. The diverse and unexpected roles of the side chain at position 66 give new insight into the chemistry of chromophore maturation in the extended family of GFP-like proteins.
Bibliography:Coordinates and structure factors have been deposited in the Protein Data Bank, access codes 1XAE (wild type) and 1XA9 (K66M).
This work was supported by NSF MCB-0111053 (to S.J.R.), NIH predoctoral traineeship (GM-00759) (to D.K.Y.), a grant for Molecular and Cellular Biology from the Russian Academy of Sciences (to K.L.), and NIH postdoctoral fellowship 1F32GM19075 (to R.M.W.).
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ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
USDOE
SLAC-REPRINT-2005-108
AC02-76SF00515
ISSN:0006-2960
1520-4995
DOI:10.1021/bi048383r