Biosensor-based micro-affinity purification for the proteomic analysis of protein complexes

J Proteome Res. 2005 Sep-Oct;4(5):1646-56. doi: 10.1021/pr050132x.

Abstract

A biosensor-based micro-affinity purification method to recover protein binding partners and their complexes for down stream proteomics analysis has been developed using the BIAcore 3000 fitted with a prototype Surface Prep Unit (SPU). The recombinant GST-intracellular domain of E-cadherin or the recombinant GST-beta-catenin binding domain of Adenomatous Polyposis Coli (APC) were immobilized onto the SPU and used to affinity purify binding partners from chromatographically enriched SW480 colon cancer cell lysates. A GST- immobilized surface was used as a control. Samples recovered from the SPU were subjected to SDS-PAGE with sensitive Coomassie staining followed by automated in-gel digestion and LC-MS/MS. The results obtained using the SPU were compared with similar experiments performed using Sepharose beads.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques*
  • Blotting, Western
  • Cadherins / chemistry
  • Cell Line, Tumor
  • Chromatography
  • Chromatography, Ion Exchange
  • Chromatography, Liquid
  • Electrophoresis, Polyacrylamide Gel
  • Glutathione Transferase / metabolism
  • Humans
  • Mass Spectrometry
  • Peptides / chemistry
  • Phosphorylation
  • Protein Binding
  • Protein Structure, Tertiary
  • Proteins / chemistry
  • Proteomics / methods*
  • Recombinant Proteins / chemistry
  • Sepharose / pharmacology
  • Time Factors
  • beta Catenin / chemistry

Substances

  • Cadherins
  • Peptides
  • Proteins
  • Recombinant Proteins
  • beta Catenin
  • Sepharose
  • Glutathione Transferase