| Literature DB >> 27086122 |
Yosuke Demizu1, Nobumichi Ohoka2, Takaya Nagakubo2, Hiroko Yamashita2, Takashi Misawa2, Keiichiro Okuhira3, Mikihiko Naito2, Masaaki Kurihara4.
Abstract
A peptide-based protein knockdown system for inducing nuclear receptors degradation via the ubiquitin-proteasome system was developed. Specifically, the designed molecules were composed of two biologically active scaffolds: a peptide that binds to the estrogen receptor α (ERα) surface and an MV1 molecule that binds to cellular inhibitors of apoptosis proteins (IAP: cIAP1/cIAP2/XIAP) to induce ubiquitylation of the ERα. The hybrid peptides induced IAP-mediated ubiquitylation followed by proteasomal degradation of the ERα. Those peptides were also applicable for inducing androgen receptor (AR) degradation.Entities:
Keywords: Helical peptide; Nuclear receptors; Protein knockdown; Protein–protein interaction
Mesh:
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Year: 2016 PMID: 27086122 DOI: 10.1016/j.bmcl.2016.04.013
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823