Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10595725 | Bioorganic & Medicinal Chemistry Letters | 2011 | 4 Pages |
Abstract
We demonstrate covalent bond formation between an RNA aptamer containing a cysteamine-tethered nucleobase and helix-threading peptides (HTPs) containing α-bromoacetamide N-termini. The reaction is high yielding and inhibited by a DNA strand Watson-Crick complementary to the aptamer sequence indicating covalent reaction is dependent on the high affinity HTP-binding site present in the folded aptamer. These results are important for future structural studies of HTP-RNA complexes and methods for the discovery of new high affinity analogs via covalent tethering strategies.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hayden Peacock, Radhika Bachu, Peter A. Beal,