4.8 Article

Genetically Encoded Tetrazine Amino Acid Directs Rapid Site-Specific in Vivo Bioorthogonal Ligation with trans-Cyclooctenes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 6, Pages 2898-2901

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja2109745

Keywords

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Funding

  1. F&M Hackman and Eyler funds [NSF-MCB-0448297]
  2. Research Corporation [CC6364, NSF-DMR-09-69301]
  3. HHMI
  4. COBRE of NCRR [P20 RR017716]
  5. NIEHS [P30ES000210]
  6. NSF CRIF:MU [CHE 0840401, CHE-0541775]
  7. Division Of Chemistry
  8. Direct For Mathematical & Physical Scien [0840401] Funding Source: National Science Foundation

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Bioorthogonal ligation methods with improved reaction rates and less obtrusive components are needed for site-specifically labeling proteins without catalysts. Currently no general method exists for in vivo site-specific labeling of proteins that combines fast reaction rate with stable, nontoxic, and chemoselective reagents. To overcome these limitations, we have developed a tetrazine-containing amino acid, 1, that is stable inside living cells. We have site-specifically genetically encoded this unique amino acid in response to an amber codon allowing a single 1 to be placed at any location in a protein. We have demonstrated that protein containing 1 can be ligated to a conformationally strained trans-cyclooctene in vitro and in vivo with reaction rates significantly faster than most commonly used labeling methods.

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