| Literature DB >> 26713108 |
Azzurra Stefanucci1, Jesús Mosquera2, Eugènio Vázquez2, José L Mascareñas2, Ettore Novellino3, Adriano Mollica4.
Abstract
ARC repressor (apoptosis repressor with caspase recruitment domain) is a protein which binds selectively to a specific sequence of DNA. In humans, ARC is primarily expressed in striated muscle tissue, which normally does not undergo rapid cell turnover. This suggests that ARC may play a protective role in the prevention against Duchenne Muscular Dystrophy and several types of tumors. In this Letter we report the synthesis, characterization, and conformational analysis of a β-sheet ARC repressor mimetic, based on the amino acid sequence of the β-sheet domain in the ARC protein. The ability of this β-sheet macrocycle to bind to double-stranded DNA was also evaluated using spectroscopic methods. Our data show that the synthetic peptide has a defined conformation and is able to bind DNA with reasonable affinity. These initial results lay the groundwork for the design of novel β-sheets folded peptides as valuable substitutes of transcription factor proteins in drug therapy.Entities:
Keywords: ARC repressor; DNA recognition; major groove; solid phase peptide synthesis; transcription factors; β-sheet macrocycles
Year: 2015 PMID: 26713108 PMCID: PMC4677364 DOI: 10.1021/acsmedchemlett.5b00363
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345