Bioconjugate Chemistry · 2007 · 27 citations · 45 references
Life SciencesBiochemistryMolecular BiologyProtein BiochemistryProtein EngineeringProteomicsCombinatorial Peptide SynthesisLigand BindingPeptide ChemistryProtein DesignProtein StructurePeptide Display LibrariesPeptide Display TechnologiesPeptide Library ConstructionPeptide Library DesignPhage Display LibrariesPhage LibrariesPhage-displayed Peptide LibrariesProtein Labeling Chemistry
A 21-mer peptide that can be used to covalently introduce synthetic molecules into proteins has been developed. Phage-displayed peptide libraries were subjected to reaction-based selection with 1,3-diketones. The peptide was further evolved by addition of a randomized region and reselection for improved binding. The resulting 21-mer peptide had a reactive amino group that formed an enaminone with 1,3-diketone and was used as a tag for labeling of maltose binding protein. Using this peptide tag and 1,3-diketone derivatives, a variety of molecules such as reporter probes and functionalities may be covalently introduced into proteins of interest.
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Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase
Irwin Chen, Mark Howarth, Weiying Lin et al. · Nature Methods · 2005 · 666 citations
Functional proteins from a random-sequence library
Anthony D. Keefe, Jack W. Szostak · Nature · 2001 · 556 citations