Informace o publikaci

Phosphorus Chemical Shifts in a Nucleic Acid Backbone from Combined Molecular Dynamics and Density Functional Calculations

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PŘECECHTĚLOVÁ Jana NOVÁK Petr MUNZAROVÁ Markéta KAUPP Martin SKLENÁŘ Vladimír

Rok publikování 2010
Druh Článek v odborném periodiku
Časopis / Zdroj The Journal of the American Chemical Society
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www http://pubs.acs.org/doi/abs/10.1021/ja104564g
Obor Fyzikální chemie a teoretická chemie
Klíčová slova MD DFT nucleic acids NMR phosphorus
Popis A comprehensive quantum chemical analysis of the influence of backbone torsion angles on 31P chemical shifts in DNAs has been carried out. An extensive DFT study employed snapshots obtained from the molecular dynamics simulation of [d(CGCGAATTCGCG)]2 to construct geometries of a hydrated dimethyl phosphate, which was used as a model for the phosphodiester linkage. Our calculations provided differences of 2.1 +/- 0.3 and 1.6 +/- 0.3 ppm between the BI and BII chemical shifts in two B-DNA residues of interest, which is in a very good agreement with the difference of 1.6 ppm inferred from experimental data. A more negative 31P chemical shift for a residue in pure BI conformation compared to residues in mixed BI/BII conformation states is provided by DFT, in agreement with the NMR experiment. Statistical analysis of the MD/DFT data revealed a large dispersion of chemical shifts in both BI and BII regions of DNA structures. 31P chemical shift ranges within 3.5 +/- 0.8 ppm in the BI region and within 4.5 +/- 1.5 ppm in the BII region. While the 31P chemical shift becomes more negative with increasing alpha in BI-DNA, it has the opposite trend in BII-DNA when both alpha and zeta increase simultaneously. The 31P chemical shift is dominated by the torsion angles alpha and zeta, while an implicit treatment of beta and epsilon is sufficient. The presence of an explicit solvent leads to a damping and a 2-3 ppm upfield shift of the torsion angle dependences.
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