Abstract
Pseudo-complementary oligonucleotide analogues and mimics provide novel opportunities for targeting duplex structures in RNA and DNA. Previously, a pseudo-complementary A-T base pair has been introduced. Towards sequence unrestricted targeting, a pseudo-complementary G-c base pair consisting of the unnatural nucleobases A/6-methoxy-2,6-diaminopurine (previously described in a DNA context) and A/4-benzoylcytosine is now presented for design of pseudo-complementary PNA oligomers (pcPNAs).
Originalsprog | Engelsk |
---|---|
Tidsskrift | Artificial DNA |
Vol/bind | 2 |
Udgave nummer | 1 |
Sider (fra-til) | 33-37 |
Antal sider | 5 |
ISSN | 1949-095X |
DOI | |
Status | Udgivet - 2011 |