Accurate representation of B-DNA double helical structure with implicit solvent and counterions

Lihua Wang, Brian E. Hingerty, A. R. Srinivasan, Wilma K. Olson, Suse Broyde

Research output: Contribution to journalArticle

Abstract

High-resolution nuclear magnetic resonance (NMR) and crystallographic data have been taken to refine the force field used in the torsion angle space nucleic acids molecular mechanics program DUPLEX. The population balance deduced from NMR studies of two carcinogen-modified DNA conformers in equilibrium was used to fine tune a sigmoidal, distance-dependent dielectric function so that reasonable relative energies could be obtained. In addition, the base-pair and backbone geometry from high-resolution crystal structures of the Dickerson-Drew dodecamer was used to re-evaluate the deoxyribose pseudorotation profile and the Lennard-Jones nonbonded energy terms. With a modified dielectric function that assumes a very steep distance-dependent form, a deoxyribose pseudorotation profile with reduced energy barriers between C2′- and C3′-endo minima, and a shift of the Lennard-Jones potential energy minimum to a distance ∼0.4 Å greater than the sum of the van der Waals' radii, the sequence-dependent conformational features of the Dickerson-Drew dodecamer in both the solid state and the aqueous liquid crystalline phase are well reproduced. The robust performance of the revised force field, in conjunction with its efficiency through implicit treatment of solvent and counterions, provides a valuable tool for elucidating conformations and structure-function relationships of DNA, including those of molecules modified by carcinogens and other ligands.

Original languageEnglish (US)
Pages (from-to)382-406
Number of pages25
JournalBiophysical journal
Volume83
Issue number1
DOIs
StatePublished - 2002

ASJC Scopus subject areas

  • Biophysics

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