A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Phosphorane intermediate vs. leaving group stabilization by intramolecular hydrogen bonding in the cleavage of trinucleoside monophosphates: implications for understanding catalysis by the large ribozymes
Tekijät: Lonnberg T, Laine M
Kustantaja: ROYAL SOC CHEMISTRY
Julkaisuvuosi: 2010
Journal: Organic and Biomolecular Chemistry
Tietokannassa oleva lehden nimi: ORGANIC & BIOMOLECULAR CHEMISTRY
Lehden akronyymi: ORG BIOMOL CHEM
Numero sarjassa: 2
Vuosikerta: 8
Numero: 2
Aloitussivu: 349
Lopetussivu: 356
Sivujen määrä: 8
ISSN: 1477-0520
DOI: https://doi.org/10.1039/b912042d
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/Publication/2774672
Hydrolysis of 2',3'-O-methyleneadenosin-5'-yl 5'-O-methyluridin-2'-yl 5'-O-methyl-2'-trifluoroacetamido-2'-deoxyuridin-3'-yl phosphate (1b) has been followed by HPLC over a wide pH range to study the effects of potential hydrogen bonding interactions of the 2'-trifluoroacetamido function on the rate and product distribution of the reaction. At pH < 2, decomposition of 1b (and its 3',3',5'-isomer 1a) is first-order in hydronium-ion concentration and cleavage of the P-O3' bond of the 2'-trifluoroacetamido-modified nucleoside is slightly favored over cleavage of the P-O5' bond. Between pH 2 and 4, the overall hydrolysis is pH-independent and the P-O3' and P-O5' bonds are cleaved at comparable rates. At pH 5, the reaction becomes first-order in hydroxide-ion concentration, with P-O3' bond cleavage predominating. At 10 mmol L(-1) aqueous sodium hydroxide, no P-O5' bond cleavage is observed. Compared to the 2'-OH counterpart 2, a modest rate enhancement is observed over the entire pH range studied. The absence of P-O5' fission under alkaline conditions suggests hydrogen bond stabilization of the departing 3'-oxyanion by the neighboring 2'-trifluoroacetamido function.
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