Rapid identification of linear protein domain binding motifs using peptide SPOT arrays

Douglas J. Briant, James M. Murphy, Genie C. Leung, Frank Sicheri

Research output: Chapter in Book/Report/Conference proceedingChapter (Book)Otherpeer-review

7 Citations (Scopus)

Abstract

Understanding protein-protein interactions is a key step in unravelling the roles proteins play in cellular function. The ability to analyse protein-protein interactions rapidly and economically is a powerful research tool. Using peptide SPOT arrays, peptides of known sequence can be synthesized directly in discrete spots on a cellulose membrane and assayed for an interaction with a protein of interest. Several hundred peptides can be synthesized on each cellulose membrane; therefore, this method is amenable to designing high-throughput peptide binding studies. SPOT arrays are particularly well suited for deducing peptidic binding motifs within proteins that are difficult to purify in sufficient quantities for traditional biochemical analyses, as well as for determining binding specificities and targets for proteins of undefined function. Peptide SPOT arrays have been used extensively to define protein-protein interaction surfaces. In this chapter, we will outline the steps involved in designing and probing a peptide SPOT array to identify peptide binding motifs for a protein of interest.

Original languageEnglish
Title of host publicationPeptide Microarrays
Subtitle of host publicationMethods and Protocols
EditorsMarina Cretich, Marcella Chiari
Place of PublicationTotowa NJ USA
PublisherHumana Press
Chapter6
Pages175-185
Number of pages11
ISBN (Print)9781603273930
DOIs
Publication statusPublished - 2009
Externally publishedYes

Publication series

NameMethods in Molecular Biology
Volume570
ISSN (Print)1064-3745

Keywords

  • identifying protein targets
  • peptide SPOT array
  • peptide synthesis
  • Protein-protein interaction

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