Correlation Between in Vitro Peptide Binding Profiles and Cellular Activities for Estrogen Receptor-Modulating Compounds

Mol Endocrinol. 2004 May;18(5):1064-81. doi: 10.1210/me.2003-0432. Epub 2004 Feb 19.


Numerous biochemical and structural studies have shown that the conformation of the estrogen receptor alpha (ERalpha) can be influenced by ligand binding. In turn, the conformational state of ERalpha affects the ability of the receptor to interact with a wide variety of protein accessory factors. To globally investigate ligand-based cofactor recruitment activities of ERalpha, we have applied a flow cytometric multiplexed binding assay to determine the simultaneous binding of ERalpha to over 50 different peptides derived from both known cofactor proteins and random peptide phage display. Using over 400 ERalpha-binding compounds, we have observed that the multiplexed in vitro peptide-binding profiles are distinct for a number of compounds and that these profiles can predict the effect that ERalpha ligands have on various cellular activities. These cell-based activities include transcriptional regulation at an estrogen response element, MCF-7 cell proliferation, and Ishikawa endometrial cell stimulation. The majority of the compound-induced diversity in the peptide profiling assay is provided by the unique phage display peptides. Importantly, some of these peptides show a sequence relationship with the corepressor motif, suggesting that peptides identified via phage display might represent natural binding partners of ERalpha. These in vitro:cellular correlations may in part explain tissue-specific activities of ERalpha-modulating compounds.

MeSH terms

  • Amino Acid Sequence
  • Cell Division / physiology*
  • Endometrium / metabolism*
  • Epithelial Cells / metabolism*
  • Estrogen Antagonists / pharmacology
  • Estrogen Receptor alpha / agonists
  • Estrogen Receptor alpha / metabolism*
  • Female
  • Humans
  • Molecular Sequence Data
  • Peptide Library
  • Peptides / metabolism*
  • Protein Conformation
  • Tumor Cells, Cultured


  • Estrogen Antagonists
  • Estrogen Receptor alpha
  • Peptide Library
  • Peptides