Publication | Open Access
Synthesis of Non-linear Protein Dimers through a Genetically Encoded Thiol-ene Reaction
16
Citations
82
References
2014
Year
Protein ChemistryFluorescent Thiol-bearing ProbeEnantioselective SynthesisNon-linear Protein DimersProtein AssemblyBiochemistryProtein FoldingNatural SciencesPeptide LibraryMolecular BiologySynthetic BiologyEscherichia ColiPeptide SynthesisProtein EngineeringMedicineStructural BiologyProtein SynthesisGenetic Encoding
Site-specific incorporation of bioorthogonal unnatural amino acids into proteins provides a useful tool for the installation of specific functionalities that will allow for the labeling of proteins with virtually any probe. We demonstrate the genetic encoding of a set of alkene lysines using the orthogonal PylRS/PylTCUA pair in Escherichia coli. The installed double bond functionality was then applied in a photoinitiated thiol-ene reaction of the protein with a fluorescent thiol-bearing probe, as well as a cysteine residue of a second protein, showing the applicability of this approach in the formation of heterogeneous non-linear fused proteins.
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