Affinity-based proteomics reveal cancer-specific networks coordinated by Hsp90 Academic Article uri icon


MeSH Major

  • Gene Expression Regulation, Neoplastic
  • HSP90 Heat-Shock Proteins
  • Neoplasms
  • Proteomics


  • Most cancers are characterized by multiple molecular alterations, but identification of the key proteins involved in these signaling pathways is currently beyond reach. We show that the inhibitor PU-H71 preferentially targets tumor-enriched Hsp90 complexes and affinity captures Hsp90-dependent oncogenic client proteins. We have used PU-H71 affinity capture to design a proteomic approach that, when combined with bioinformatic pathway analysis, identifies dysregulated signaling networks and key oncoproteins in chronic myeloid leukemia. The identified interactome overlaps with the well-characterized altered proteome in this cancer, indicating that this method can provide global insights into the biology of individual tumors, including primary patient specimens. In addition, we show that this approach can be used to identify previously uncharacterized oncoproteins and mechanisms, potentially leading to new targeted therapies. We further show that the abundance of the PU-H71-enriched Hsp90 species, which is not dictated by Hsp90 expression alone, is predictive of the cell's sensitivity to Hsp90 inhibition.

publication date

  • November 2011



  • Academic Article



  • eng

PubMed Central ID

  • PMC3265389

Digital Object Identifier (DOI)

  • 10.1038/nchembio.670

PubMed ID

  • 21946277

Additional Document Info

start page

  • 818

end page

  • 26


  • 7


  • 11