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 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
American Chemical Society
11-01-2005
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Subjects: | |
Online Access: | Get full text |
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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. |
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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.). istex:2C5DFF1EA54C4510695D9194C643BE3CF67343A1 ark:/67375/TPS-268CLM10-4 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 |