Unnatural base pairs mediate the site-specific incorporation of an unnatural hydrophobic component into RNA transcripts

Abstract

Site-specific incorporation of a hydrophobic nucleotide analog into RNA, by T7 transcription mediated by unnatural base pairs, was developed. The nucleotide analog, 5-phenylethynyl-3-(β- d-ribofuranosyl)pyridin-2-one 5-triphosphate (denoted by Ph- yTP), was chemically synthesized and then site-specifically incorporated by T7 RNA polymerase into RNA opposite the pairing partner, 2-amino-6-(2-thienyl)purine (denoted by s) in DNA templates. The introduction of Ph- y into a theophylline-binding RNA aptamer, in which a uridine in the internal loop was replaced by Ph- y, raised the thermal stability of the aptamer. Thus, this unnatural nucleotide analog would be useful for stabilizing RNA tertiary structures and complexes between RNA and other molecules.