Cyclic Peptides Incorporating Phosphotyrosine Mimetics as Potent and Specific Inhibitors of the Grb7 Breast Cancer Target.
| Autor: | Watson GM, Gunzburg MJ, Ambaye ND, Lucas WA, Traore DA, Kulkarni K, Cergol KM; School of Chemistry, The University of Sydney , Sydney, New South Wales 2006, Australia., Payne RJ; School of Chemistry, The University of Sydney , Sydney, New South Wales 2006, Australia., Panjikar S; Australian Synchrotron , 800 Blackburn Road, Clayton, Victoria 3168, Australia., Pero SC; Department of Surgery and Vermont Cancer Center, University of Vermont , Burlington, Vermont 05401, United States., Perlmutter P, Wilce MC, Wilce JA |
|---|---|
| Jazyk: | angličtina |
| Zdroj: | Journal of medicinal chemistry [J Med Chem] 2015 Oct 08; Vol. 58 (19), pp. 7707-18. Date of Electronic Publication: 2015 Sep 23. |
| DOI: | 10.1021/acs.jmedchem.5b00609 |
| Abstrakt: | The Grb7 adaptor protein is a therapeutic target for both TNBC and HER2+ breast cancer. A nonphosphorylated cyclic peptide 1 (known as G7-18NATE) inhibits Grb7 via targeting the Grb7-SH2 domain, but requires the presence of phosphate ions for both affinity and specificity. Here we report the discovery of malonate bound in the phosphotyrosine binding pocket of the apo-Grb7-SH2 structure. Based on this, we carried out the rational design and synthesis of two analogues of peptide 1 that incorporate carboxymethylphenylalanine (cmF) and carboxyphenylalanine (cF) as mimics of phosphotyrosine (pY). Binding studies using SPR confirmed that affinity for Grb7-SH2 domain is improved up to 9-fold over peptide 1 under physiological phosphate conditions (KD = 2.1-5.7 μM) and that binding is specific for Grb7-SH2 over closely related domains (low or no detectable binding to Grb2-SH2 and Grb10-SH2). X-ray crystallographic structural analysis of the analogue bearing a cmF moiety in complex with Grb7-SH2 has identified the precise contacts conferred by the pY mimic that underpin this improved molecular interaction. Together this study identifies and characterizes the tightest specific inhibitor of Grb7 to date, representing a significant development toward a new Grb7-targeted therapeutic. |
| Databáze: | MEDLINE |
| Externí odkaz: |
|