2-Aminophenanthroline dimer stabilized the C-C mismatched duplex DNA.

Bioorg Med Chem

Department of Regulatory Bioorganic Chemistry, The Institute of Scientific and Industrial Research (ISIR), Osaka University, Ibaraki 567-0047, Japan. Electronic address:

Published: February 2015

New ligands with three-ring system for the recognition of a cytosine bulge and a cytosine-cytosine mismatch were designed and synthesized. The 2-amino-1,10-phenanthroline was selected as a recognition unit among the possible three-ring systems of a parent recognition unit of 2-amino-1,8-naphthyridine. The 3-aminopropanamide of 2-amino-1,10-phenanthroline (APM) bound to the cytosine bulge DNA. Other single nucleotide bulges were stabilized by the ligand with much lower efficiency. The dimer APD consisting of two molecules of APM was found to stabilize the C-C mismatch DNA selectively. Structure-activity relationship studies revealed that the APD-binding to the C-C mismatch DNA required both phenanthroline heterocycles in a molecule.

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http://dx.doi.org/10.1016/j.bmc.2014.12.062DOI Listing

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