The use of phage display in neurobiology

Curr Protoc Neurosci. 2010 Apr:Chapter 5:Unit 5.12. doi: 10.1002/0471142301.ns0512s51.

Abstract

Phage display has been extensively used to study protein-protein interactions, receptor- and antibody-binding sites, and immune responses, to modify protein properties, and to select antibodies against a wide range of different antigens. In the format most often used, a polypeptide is displayed on the surface of a filamentous phage by genetic fusion to one of the coat proteins, creating a chimeric coat protein, and coupling phenotype (the protein) to genotype (the gene within). As the gene encoding the chimeric coat protein is packaged within the phage, selection of the phage on the basis of the binding properties of the polypeptide displayed on the surface simultaneously results in the isolation of the gene encoding the polypeptide. This unit describes the background to the technique, and illustrates how it has been applied to a number of different problems, each of which has its neurobiological counterparts. Although this overview concentrates on the use of filamentous phage, which is the most popular platform, other systems are also described.

Publication types

  • Review

MeSH terms

  • Animals
  • Antibodies / genetics
  • Antibodies / isolation & purification
  • Bacteriophages / genetics*
  • Bacteriophages / immunology
  • Bacteriophages / metabolism
  • Genes, Viral / genetics
  • Genetic Vectors / genetics*
  • Humans
  • Ligands
  • Neurobiology / methods*
  • Peptide Library*
  • Peptides / genetics
  • Peptides / metabolism
  • Protein Binding / physiology
  • Recombinant Fusion Proteins / genetics*
  • Recombinant Fusion Proteins / immunology
  • Recombinant Fusion Proteins / metabolism

Substances

  • Antibodies
  • Ligands
  • Peptide Library
  • Peptides
  • Recombinant Fusion Proteins