4.5 Review

Genetic code expansion and bioorthogonal labelling enables cell specific proteomics in an animal

Journal

CURRENT OPINION IN CHEMICAL BIOLOGY
Volume 21, Issue -, Pages 154-160

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2014.07.001

Keywords

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Funding

  1. Medical Research Council [U105181009, UD99999908]
  2. Louis Jeantet Young Investigator Award
  3. ERC
  4. MRC [MC_UP_A024_1008] Funding Source: UKRI
  5. Medical Research Council [MC_UP_A024_1008] Funding Source: researchfish

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The site specific, co-translational introduction of unnatural amino acids into proteins produced in cells has been facilitated by the development of the pyrrolysyl-tRNA synthetase/tRNA(CUA) pair. This pair can now be used to direct the site-specific incorporation of designer amino acids in E. coli, yeast, mammalian cells, and animals (the worm, C. elegans and the fly, D. melanogaster). Developments in encoding components of rapid bioorthogonal reactions are providing new opportunities for labelling and visualising proteins. A new method called stochastic orthogonal recoding of translation with chemoselective modification (SORT-M) leverages advances in genetic code expansion and bioorthogonal chemistry to label proteomes with diverse chemistry at diverse codons in E coli, mammalian cells, and in spatially and temporally defined sets of cells in the fly. Proteomes in targeted sets of cells have been visualised by SORT-M and proteins in targeted cells have been identified by SORT-M.

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