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Published April 19, 2001 | Supplemental Material
Journal Article Open

Fmoc solid phase synthesis of polyamides containing pyrrole and imidazole amino acids

Abstract

Polyamides containing N-methylimidazole (Im) and N-methylpyrrole (Py) amino acids are synthetic ligands that have an affinity and specificity for DNA comparable to those of many naturally occurring DNA binding proteins. A machine-assisted Fmoc solid phase synthesis of polyamides has been optimized to afford high stepwise coupling yields (>99%). Two monomer building blocks, Fmoc-Py acid and Fmoc-Im acid, were prepared in multigram scale. Cleavage by aminolysis followed by HPLC purification affords up to 200 mg quantities of polyamide with purities and yields greater than or equal to those reported using Boc chemistry. A broader set of reaction conditions will increase the number and complexity of minor groove binding polyamides which may be prepared and help ensure compatibility with many commercially available peptide synthesizers.

Additional Information

© 2001 American Chemical Society. Received February 7, 2001; Publication Date (Web): March 28, 2001. We are grateful to the National Institute of Health for research support, the Ralph M. Parsons Foundation for a predoctoral fellowship for N.R.W., J. Edward Richter for an undergraduate fellowship to J.M.T., and the Howard Hughes Medical Institute for a predoctoral fellowship to E.E.B.

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