A targeted proteomic approach for the identification of tumor-associated membrane antigens using the ProteomeLab PF-2D in tandem with mass spectrometry

Biochem Biophys Res Commun. 2006 Sep 29;348(3):1055-62. doi: 10.1016/j.bbrc.2006.07.187. Epub 2006 Aug 7.

Abstract

Mapping differential expression of soluble proteins has become fairly routine using chromatofocusing in combination with the reversed-phase HPLC (ProteomeLab PF-2D by Beckman Coulter Inc.); however, identification of membrane antigens has not been reported thus far. In this report, we demonstrate a targeted proteomic approach employing immunoprecipitation, prior to 2D-LC separation, in tandem with MS/MS that can be used to identify tumor-associated membrane antigens. This system is very sensitive and reproducible in that only 1/4th the amount of starting material is required for analysis as compared to gel-based analysis, and permits a focused environment for eliminating non-specific interactions leading to an accurate resolution of the cognate antigen. This system also circumvents the well-known limitations associated with gel-based approaches. This approach has been validated in the identification of ErB2/HER-2 and was subsequently used to identify CD44E as the cognate antigen for VB1-008, one of our fully human, tumor-specific, monoclonal antibodies.

Publication types

  • Validation Study

MeSH terms

  • Antibodies, Monoclonal / metabolism
  • Antibodies, Neoplasm / metabolism
  • Antigens, Neoplasm / analysis*
  • Antigens, Neoplasm / immunology
  • Antigens, Neoplasm / metabolism
  • Binding Sites, Antibody
  • Blotting, Western
  • Cell Line, Tumor
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • Mass Spectrometry
  • Membrane Proteins / analysis*
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism
  • Neoplasm Proteins / analysis*
  • Neoplasm Proteins / immunology
  • Neoplasm Proteins / metabolism
  • Proteome / analysis*
  • Proteome / immunology
  • Proteome / metabolism
  • Receptor, ErbB-2 / chemistry
  • Receptor, ErbB-2 / isolation & purification

Substances

  • Antibodies, Monoclonal
  • Antibodies, Neoplasm
  • Antigens, Neoplasm
  • Membrane Proteins
  • Neoplasm Proteins
  • Proteome
  • Receptor, ErbB-2