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J Am Chem Soc. 2014 Aug 13;136(32):11232-5. doi: 10.1021/ja504076t. Epub 2014 Jul 30.

Inhibiting epidermal growth factor receptor at a distance.

Author information

1
Department of Chemistry and ‡Department of Molecular, Cellular and Developmental Biology, Yale University , New Haven, Connecticut 06520-8107, United States.

Abstract

The epidermal growth factor receptor (EGFR) tyrosine kinase is implicated in a large number of human cancers. Most EGFR inhibitors target the extracellular, growth factor-binding domain or the intracellular, ATP-binding domain. Here we describe molecules that inhibit the kinase activity of EGFR in a new way, by competing with formation of an essential intradimer coiled coil containing the juxtamembrane segment from each member of the receptor partnership. The most potent molecules we describe bind EGFR directly, decrease the proliferation of wild-type and mutant EGFR-dependent cells lines, inhibit phosphorylation of EGFR and downstream targets, and block coiled coil formation as judged by bipartite tetracysteine display. Potency is directly correlated with the ability to block coiled coil formation within full-length EGFR in cells.

PMID:
25075632
PMCID:
PMC4140499
DOI:
10.1021/ja504076t
[Indexed for MEDLINE]
Free PMC Article

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