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Energetic preference of 8-oxoG eversion pathways in a DNA glycosylase

  • Christina Bergonzo
  • , Arthur J. Campbell
  • , Carlos De Los Santos
  • , Arthur P. Grollman
  • , Carlos Simmerling
  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Base eversion is a fundamental process in the biochemistry of nucleic acids, allowing proteins engaged in DNA repair and epigenetic modifications to access target bases in DNA. Crystal structures reveal end points of these processes, but not the pathways involved in the dynamic process of base recognition. To elucidate the pathway taken by 8-oxoguanine during base excision repair by Fpg, we calculated free energy surfaces during eversion of the damaged base through the major and minor grooves. The minor groove pathway and free energy barrier (6-7 kcal/mol) are consistent with previously reported results (Qi, Y.; Spong, M. C.; Nam, K.; Banerjee, A.; Jiralerspong, S.; Karplus, M.; Verdine, G. L. Nature2009, 462, 762.) However, eversion of 8-oxoG through the major groove encounters a significantly lower barrier (3-4 kcal/mol) more consistent with experimentally determined rates of enzymatic sliding during lesion search (Blainey, P. C.; van Oijent, A. M.; Banerjee, A.; Verdine, G. L.; Xie, X. S. Proc. Natl. Acad. Sci. U.S.A.2006, 103, 5752.). Major groove eversion has been suggested for other glycosylases, suggesting that in addition to function, dynamics of base eversion may also be conserved.

Original languageEnglish
Pages (from-to)14504-14506
Number of pages3
JournalJournal of the American Chemical Society
Volume133
Issue number37
DOIs
StatePublished - Sep 21 2011

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