A1 Journal article – refereed
Phosphorane intermediate vs. leaving group stabilization by intramolecular hydrogen bonding in the cleavage of trinucleoside monophosphates: implications for understanding catalysis by the large ribozymes




List of Authors: Lonnberg T, Laine M
Publisher: ROYAL SOC CHEMISTRY
Publication year: 2010
Journal: Organic and Biomolecular Chemistry
Journal name in source: ORGANIC & BIOMOLECULAR CHEMISTRY
Journal acronym: ORG BIOMOL CHEM
Number in series: 2
Volume number: 8
Issue number: 2
Number of pages: 8
ISSN: 1477-0520

Abstract
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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Last updated on 2019-21-08 at 20:40