Stereospecific effects determine the structure of a four-way DNA junction

Jia Liu, Anne-Cécile Déclais, Sean A. McKinney, Taekjip Ha, David G. Norman, David M. J. Lilley (Lead / Corresponding author)

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Conversion of a centrally located phosphate group to an electrically neutral methyl phosphonate in a four-way DNA junction can exert a major influence on its conformation. However, the effect is strongly dependent on stereochemistry. Substitution of the proR oxygen atom by methyl leads to conformational transition to the stacking conformer that places this phosphate at the point of strand exchange. By contrast, corresponding modification of the proS oxygen destabilizes this conformation of the junction. Single-molecule analysis shows that both molecules are in a dynamic equilibrium between alternative stacking conformers, but the configuration of the methyl phosphonate determines the bias of the conformational equilibrium. It is likely that the stereochemical environment of the methyl group affects the interaction with metal ions in the center of the junction.
Original languageEnglish
Pages (from-to)217-228
Number of pages12
JournalChemistry & Biology
Volume12
Issue number2
DOIs
Publication statusPublished - 2005

Keywords

  • Stereochemistry
  • Metal ions
  • DNA
  • RNA folding

Fingerprint Dive into the research topics of 'Stereospecific effects determine the structure of a four-way DNA junction'. Together they form a unique fingerprint.

  • Cite this