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Published October 21, 2011 | Published + Supplemental Material
Journal Article Open

Expanding the Repertoire of Natural Product-Inspired Ring Pairs for Molecular Recognition of DNA

Abstract

A furan amino acid, inspired by the recently discovered proximicin natural products, was incorporated into the scaffold of a DNA-binding hairpin polyamide. While unpaired oligomers of 2,4-disubstituted furan amino acids show poor DNA-binding activity, furan (Fn) carboxamides paired with N-methylpyrrole (Py) and N-methylimidazole (Im) rings demonstrate excellent stabilization of duplex DNA as well as discrimination of noncognate sequences, consistent with function as a Py mimic according to the Py/Im polyamide pairing rules.

Additional Information

© 2011 American Chemical Society. ACS AuthorChoice. Received August 30, 2011. Publication Date (Web): September 29, 2011. We are grateful to the National Institutes of Health(GM27681) for research support. J.L.M. (PF-10-015-01-CDD) and D.A.G. (PF-09-262-01-CDD) were supported by postdoctoral fellowships from the American Cancer Society. J.A.R. was supported by an Alexander von Humboldt postdoctoral fellowship.

Attached Files

Published - Muzikar2011p16279Org_Lett.pdf

Supplemental Material - ol202285y_si_001.pdf

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