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Aminoethylprolyl peptide nucleic acids (aepPNA): chiral PNA analogues that form highly stable DNA:aepPNA2 triplexes
M D'Costa1, V A Kumar, K N Ganesh
1Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune, India.
Organic Letters
|June 3, 2000
Abstract:
[formula: see text] The replacement of the glycyl component in the peptide nucleic acid (PNA) backbone by a prolyl unit bearing a nucleobase leads to the aminoethylprolyl (aep) PNAs, which are chiral and cationic. The homooligomeric aepPNA binds to complementary DNA sequences with high affinity and sequence specificity, forming highly stable triplexes.