Electrostatic energy analysis of 8-oxoguanine DNA lesion--molecular dynamics study

One nanosecond molecular dynamics (MD) simulation was performed for two DNA segments each composed of 30 base pairs. In one DNA segment the native guanines at nucleotides positions 17 and 19 were replaced with two 8-oxoguanines (8-oxoG) (8-oxoG is mutagenic DNA oxo-lesion). The analysis of results was focused on the electrostatic energy that is supposed to be significant factor causing the disruption of DNA base stacking in DNA duplex and may also serve as a signal toward the repair enzyme informing the presence of the lesion. The repulsive interaction between 8-oxoG and the entire DNA molecule was observed, which caused the extrahelical position of 8-oxoG (position 19). The repulsive electrostatic interaction between both 8-oxoG lesions contributed to the flipping out of one 8-oxoG and to the local instability of the lesioned DNA region. The electrostatic potential at the surface of DNA close to the lesions has more negative value than the same region on the native DNA. This electrostatic potential may signal presence of the lesion to the repair enzyme. In the simulation of native DNA segment, no significant structural changes were observed and B-DNA structure was well preserved throughout the MD simulation.

[1]  B. Honig,et al.  Calculation of electrostatic potentials in an enzyme active site , 1987, Nature.

[2]  R. Lloyd,et al.  Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli. , 2001, Nucleic acids research.

[3]  Richard A. Friesner,et al.  Accurate ab Initio Quantum Chemical Determination of the Relative Energetics of Peptide Conformations and Assessment of Empirical Force Fields , 1997 .

[4]  T. Darden,et al.  Particle mesh Ewald: An N⋅log(N) method for Ewald sums in large systems , 1993 .

[5]  P. Kollman,et al.  A well-behaved electrostatic potential-based method using charge restraints for deriving atomic char , 1993 .

[6]  William Arbuthnot Sir Lane,et al.  The critical active-site amine of the human 8-oxoguanine DNA glycosylase, hOgg1: direct identification, ablation and chemical reconstitution. , 1997, Chemistry & biology.

[7]  D. Shortle,et al.  Mutational studies of protein structures and their stabilities , 1992, Quarterly Reviews of Biophysics.

[8]  S. Harrison,et al.  DNA recognition by proteins with the helix-turn-helix motif. , 1990, Annual review of biochemistry.

[9]  B. Honig,et al.  Classical electrostatics in biology and chemistry. , 1995, Science.

[10]  José L. F. Abascal,et al.  Ionic distribution around simple B-DNA models. III. The effect of ionic charge , 2001 .

[11]  Gene regulation by steroid hormones , 1989, Cell.

[12]  P. Webb,et al.  Characterization of response elements for androgens, glucocorticoids and progestins in mouse mammary tumour virus. , 1988, Nucleic acids research.

[13]  Miroslav Pinak Hydration at the TD Damaged Site of DNA and its Role in the Formation of Complex with T4 Endonuclease V , 2000 .

[14]  An-Suei Yang,et al.  Electrostatic effects on protein stability: Current Opinion in Structural Biology 1992, 2:40…-45 , 1992 .

[15]  P. Kollman,et al.  A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic Molecules , 1995 .

[16]  Wilfred F. van Gunsteren,et al.  Computer Simulation of Biomolecular Systems: Theoretical and Experimental Applications , 1989 .

[17]  G. Dianov,et al.  Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells. , 1999, Nucleic acids research.

[18]  U. Landman,et al.  Charge Migration in DNA: Ion-Gated Transport , 2001, Science.

[19]  Thierry Soussi,et al.  Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation , 1996, Nucleic Acids Res..