Literature DB >> 23788558

Specificity profiling of protein-binding domains using one-bead-one-compound Peptide libraries.

Andrew R Kunys1, Wenlong Lian, Dehua Pei.   

Abstract

One-bead-one-compound (OBOC) libraries consist of structurally related compounds (e.g., peptides) covalently attached to a solid support, with each resin bead carrying a unique compound. OBOC libraries of high structural diversity can be rapidly synthesized and screened without the need for any special equipment, and therefore can be employed in any chemical or biochemical laboratory. OBOC peptide libraries have been widely used to map the ligand specificity of proteins, to determine the substrate specificity of enzymes, and to develop inhibitors against macromolecular targets. They have proven particularly useful in profiling the binding specificity of protein modular domains (e.g., SH2 domains, BIR domains, and PDZ domains); subsequently, the specificity information can be used to predict the protein targets of these domains. The protocols outlined in this article describe the methodologies for synthesizing and screening OBOC peptide libraries against SH2 and PDZ domains, and the related data analysis. Curr. Protoc. Chem. Biol. 4:331-355
© 2012 by John Wiley & Sons, Inc.

Entities:  

Keywords:  SH2 domains; one‐bead‐one‐compound libraries; peptide libraries; protein binding domains; protein‐protein interaction; sequence specificity

Year:  2012        PMID: 23788558      PMCID: PMC3690186          DOI: 10.1002/9780470559277.ch120125

Source DB:  PubMed          Journal:  Curr Protoc Chem Biol        ISSN: 2160-4762


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