KINETICALLY SELECTIVE BINDING OF SINGLE STRANDED RNA OVER DNA BY A PYRROLIDINE-AMIDE OLIGONUCLEOTIDE MIMIC (POM)
David T. Hickman, Paul M. King, Jonathan M. Slater, Matthew A. Cooper, Jason Micklefield
Abstract
David T. Hickman, Paul M. King, Jonathan M. Slater, Matthew A. Cooper, Jason Micklefield
Abstract
Replacing the sugar-phosphodiester backbone of nucleic acids with a pyrrolidine-amide backbone results in an oligonucleotide mimic POM 1 which binds with high affinity and specificity to complementary DNA and RNA. Unlike other modified oligonucleotides, POM binds much more rapidly to single stranded RNA than DNA.
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Replacing the sugar-phosphodiester backbone of nucleic acids with a pyrrolidine-amide backbone results in an oligonucleotide mimic POM 1 which binds with high affinity and specificity to complementary DNA and RNA. Unlike other modified oligonucleotides, POM binds much more rapidly to single stranded RNA than DNA.
Key concepts: Phosphodiester bond, Oligonucleotide, Pyrrolidine, DNA, RNA, Chemistry, Nucleic acid, Amide