ACS Medicinal Chemistry Letters · 2015 · 20 citations · 28 references
Life SciencesBiochemistryMolecular BiologyDrug DesignStructural BiochemistryStructural BiologyMacromolecular StructurePeptide Drug DiscoveryProtein DesignProtein StructureStructural DomainsBeta SheetsBeta-sheet AnalysisCaspase Recruitment DomainsDouble-stranded Dna RecognitionDouble-stranded Dna StructureMacrocyclic PeptidesSynthetic Peptide AnalogsSynthetic Peptide Characterization
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.
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DNA recognition by β-sheets in the Arc represser–operator crystal structure
Brigitte E. Raumann, Mark A. Rould, Carl O. Pabo et al. · Nature · 1994 · 260 citations
DNA sequence dependent binding modes of 4',6-diamidino-2-phenylindole (DAPI)
W. David Wilson, Farial A. Tanious, H. Bartoń et al. · Biochemistry · 1990 · 218 citations