B1 Vertaisarvioimaton kirjoitus tieteellisessä lehdessä
Sequence-selective cleavage of oligoribonucleotides
Tekijät: Niittymaki T, Lonnberg H
Julkaisuvuosi: 2005
Lehti:: Collection Symposium Series
Tietokannassa oleva lehden nimi: Chemistry of Nucleic Acid Components
Lehden akronyymi: COLL SYMPOS SERIES
Vuosikerta: 7
Aloitussivu: 443
Lopetussivu: 444
Sivujen määrä: 2
ISBN: 80-86241-25-4
Tiivistelmä
2'-O-Methyl oligoribonucleotides bearing a 1,5,9-triazacyclododec-3-yl group tethered either to the 3'-terminus of an oligonucleotide or to an intrachain abasic sugar unit have been shown to cleave in slight excess of Zn2+, ions complementary oligoribonucleotides. The cleavage obeys first-order kinetics and exhibits turnover. The accelaration compared to the monomeric Zn2+ 1,5,9-triazacyclododecane chelate is more than 100-fold for the 3'-tethered conjugates and approximately 50-fold for the intrachain conjugates.
2'-O-Methyl oligoribonucleotides bearing a 1,5,9-triazacyclododec-3-yl group tethered either to the 3'-terminus of an oligonucleotide or to an intrachain abasic sugar unit have been shown to cleave in slight excess of Zn2+, ions complementary oligoribonucleotides. The cleavage obeys first-order kinetics and exhibits turnover. The accelaration compared to the monomeric Zn2+ 1,5,9-triazacyclododecane chelate is more than 100-fold for the 3'-tethered conjugates and approximately 50-fold for the intrachain conjugates.