Publication | Closed Access
Mapping Protease Substrates by Using a Biotinylated Phage Substrate Library
48
Citations
17
References
2006
Year
Protein AssemblyPeptide EngineeringProteasomeMolecular BiologyBira SubstrateCombinatorial Heptamer PeptidesProtein FoldingProteomicsProtein ChemistryBiochemistryProkaryotic VirusStructural BiologyBiomolecular EngineeringNatural SciencesPeptide LibraryProtease CleavageBiotechnologyProtease SubstratesEnzyme SpecificityPeptide SynthesisProtein EngineeringMedicine
We describe a bacteriophage M13 substrate library encoding the AviTag (BirA substrate) and combinatorial heptamer peptides displayed at the N terminus of the mature form of capsid protein III. Phages are biotinylated efficiently (> or = 50%) when grown in E. coli cells coexpressing BirA, and such viral particles can be immobilized on a streptavidin-coated support and released by protease cleavage within the combinatorial peptide. We have used this library to map the specificity of human Factor Xa and a neuropeptidase, neurolysin (EC3.4.24.16). Validation by analysis of isolated peptide substrates has revealed that neurolysin recognizes the motif hydrophobic-X-Pro-Arg-hydrophobic, where Arg-hydrophobic is the scissile bond.
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