Journal article
Genetic incorporation of olefin cross-metathesis reaction tags for protein modification
- Abstract:
- Olefin cross-metathesis (CM) is a viable reaction for the modification of alkene-containing proteins. Although allyl sulfide or selenide side-chain motifs in proteins can critically enhance the rate of CM reactions, no efficient method for their site-selective genetic incorporation into proteins has been reported to date. Here, through the systematic evaluation of olefin-bearing unnatural amino acids for their metabolic incorporation, we have discovered S-allylhomocysteine (Ahc) as a genetically encodable Met analogue that is not only processed by translational cellular machinery but also a privileged CM substrate residue in proteins. In this way, Ahc was used for efficient Met codon reassignment in a Met-auxotrophic strain of E. coli (B834 (DE3)) as well as metabolic labeling of protein in human cells and was reactive toward CM in several representative proteins. This expands the use of CM in the toolkit for "tag-and-modify" functionalization of proteins.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 4.6MB, Terms of use)
-
- Publisher copy:
- 10.1021/jacs.8b09433
Authors
+ Royal Society
More from this funder
- Funding agency for:
- Davis, B
- Grant:
- Wolfson Research Merit Award
- Publisher:
- American Chemical Society
- Journal:
- Journal of the American Chemical Society More from this journal
- Volume:
- 140
- Issue:
- 44
- Pages:
- 14599-14603
- Publication date:
- 2018-10-16
- Acceptance date:
- 2018-10-16
- DOI:
- EISSN:
-
1520-5126
- ISSN:
-
0002-7863
- Pmid:
-
30371070
- Language:
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English
- Pubs id:
-
pubs:935835
- UUID:
-
uuid:37436f1d-1c5b-46f1-8a9f-a295d54677ce
- Local pid:
-
pubs:935835
- Source identifiers:
-
935835
- Deposit date:
-
2018-12-16
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2018
- Notes:
- Copyright © 2018 American Chemical Society. This is the accepted manuscript version of the article. The final version is available online from American Chemical Society at: https://doi.org/10.1021/jacs.8b09433
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