| HENNIG, Mirko, Marketa MUNZAROVA, Wolfgang BERMEL, Lincol G. SCOTT, Vladimir SKLENAR and James R. WILLIAMSON. Measurement of Long Range 1H-19F Scalar Coupling Constants and their Glycosidic Torsion Dependence in 5-Fluoropyrimidine Substituted RNA. (Three-Bond Sugar-Base Couplings in Purine versus Pyrimidine Nucleosides: A DFT Study of Karplus Relationships for 3JC2/4-H1' and 3JC6/8-H1' in DNA). Journal of the American Chemical Society. Washington, D.C.: American Chemical Society, 2006, vol. 128, No 17, p. 5851-5858. ISSN 0002-7863. |
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@article{634894,
author = {Hennig, Mirko and Munzarova, Marketa and Bermel, Wolfgang and Scott, Lincol G. and Sklenar, Vladimir and Williamson, James R.},
article_location = {Washington, D.C.},
article_number = {17},
keywords = {Scalar Coupling Constants; Fluorine; 5-Fluorouridine; 5-Fluorocytidine; HIV-TAR RNA},
language = {eng},
issn = {0002-7863},
journal = {Journal of the American Chemical Society},
title = {Measurement of Long Range 1H-19F Scalar Coupling Constants and their Glycosidic Torsion Dependence in 5-Fluoropyrimidine Substituted RNA.},
volume = {128},
year = {2006}
}
TY - JOUR
ID - 634894
AU - Hennig, Mirko - Munzarova, Marketa - Bermel, Wolfgang - Scott, Lincol G. - Sklenar, Vladimir - Williamson, James R.
PY - 2006
TI - Measurement of Long Range 1H-19F Scalar Coupling Constants and their Glycosidic Torsion Dependence in 5-Fluoropyrimidine Substituted RNA.
JF - Journal of the American Chemical Society
VL - 128
IS - 17
SP - 5851-5858
EP - 5851-5858
PB - American Chemical Society
SN - 00027863
KW - Scalar Coupling Constants
KW - Fluorine
KW - 5-Fluorouridine
KW - 5-Fluorocytidine
KW - HIV-TAR RNA
N2 - Long range scalar 5J(H1',F) couplings were observed in 5-fluoropyrimidine substituted RNA. We developed a novel S3E-19F-alfa/beta-edited NOESY experiment for quantitation of these long range scalar 5J(H1',F), where the J-couplings can be extracted from inspection of intraresidual (H1',H6) NOE crosspeaks. The 5J(H1',F) couplings can be used to restrict the glycosidic torsion angle which defines the orientation of the base with respect to the ribose sugar moiety. Quantum chemical calculations were exploited to investigate the relation between scalar couplings and conformations around the glycosidic bond in oligonucleotides. The theoretical dependence of the observed 5J(H1',F) couplings on the torsion angle Ó can be described by a generalized Karplus relationship. The corresponding density functional theory (DFT) analysis is outlined. Additional NMR experiments facilitating the resonance assignments of 5-fluoropyrimidine substituted RNAs are described and chemical shift changes due to altered shielding in the presence of fluorine-19 (19F) are presented.
ER -
HENNIG, Mirko, Marketa MUNZAROVA, Wolfgang BERMEL, Lincol G. SCOTT, Vladimir SKLENAR and James R. WILLIAMSON. Measurement of Long Range 1H-19F Scalar Coupling Constants and their Glycosidic Torsion Dependence in 5-Fluoropyrimidine Substituted RNA. (Three-Bond Sugar-Base Couplings in Purine versus Pyrimidine Nucleosides: A DFT Study of Karplus Relationships for 3JC2/4-H1' and 3JC6/8-H1' in DNA). \textit{Journal of the American Chemical Society}. Washington, D.C.: American Chemical Society, 2006, vol.~128, No~17, p.~5851-5858. ISSN~0002-7863.
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