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Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells
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Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells

Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells

DOI:
10.3791/57069-v

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14:02 min

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April 09, 2018

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, , ,
1Institute of Biochemistry, Faculty of Life Sciences,University of Leipzig

Capitoli

  • 00:04Titolo
  • 01:11Fluorescence-based Screening of Incorporation Efficiencies
  • 04:22Genetic Incorporation of ncAAs into GPCRs
  • 08:21Ultrafast Bioorthogonal Labeling of GPCRs on Live Mammalian Cells
  • 11:11Results: Incorporation of Chemical Probes into GPCRs in Mammalian Cells for Cross-linking and Imaging Studies
  • 12:52Conclusion

Summary

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Traduzione automatica

A facile fluorescence assay is presented to evaluate the efficiency of amino-acyl-tRNA-synthetase/tRNA pairs incorporating non-canonical amino-acids (ncAAs) into proteins expressed in mammalian cells. The application of ncAAs to study G-protein coupled receptors (GPCRs) is described, including photo-crosslinking mapping of binding sites and bioorthogonal GPCR labeling on live cells.

Tags

GPCRPhoto-crosslinkingBioorthogonal ChemistryNon-canonical Amino AcidsAmber Codon SuppressionFluorescence AssayMammalian CellsProtein-protein InteractionsLigand BindingLive Cell Imaging

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