4.8 Article

2′-Alkynyl spin-labelling is a minimally perturbing tool for DNA structural analysis

Journal

NUCLEIC ACIDS RESEARCH
Volume 48, Issue 6, Pages 2830-2840

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkaa086

Keywords

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Funding

  1. Engineering and Physical Sciences Research Council [EP/M019195/1]
  2. Engineering and Physical Sciences Research Council Studentship
  3. Biotechnology and Biological Sciences Research Council [BB/J001694/2, BB/R021848/1]
  4. ADTBio
  5. University of Kentucky
  6. NCI Cancer Center Support Grant [P30 CA177558]
  7. Carmen L. Buck Endowment
  8. Emerging Fields Initiative of the Friedrich-Alexander-University of ErlangenNuremberg [Grant title 'Chemistry in Live Cells']
  9. Wellcome Trust [099149/Z/12/Z]
  10. Royal Society, University Research Fellowship
  11. University of Oxford
  12. BBSRC [BB/R021848/1, BB/J001694/2] Funding Source: UKRI
  13. EPSRC [EP/M019195/1] Funding Source: UKRI

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The determination of distances between specific points in nucleic acids is essential to understanding their behaviour at the molecular level. The ability to measure distances of 2-10 nm is particularly important: deformations arising from protein binding commonly fall within this range, but the reliable measurement of such distances for a conformational ensemble remains a significant challenge. Using several techniques, we show that electron paramagnetic resonance (EPR) spectroscopy of oligonucleotides spin-labelled with triazole-appended nitroxides at the 2' position offers a robust and minimally perturbing tool for obtaining such measurements. For two nitroxides, we present results from EPR spectroscopy, X-ray crystal structures of B-form spin-labelled DNA duplexes, molecular dynamics simulations and nuclear magnetic resonance spectroscopy. These four methods are mutually supportive, and pinpoint the locations of the spin labels on the duplexes. In doing so, this work establishes 2'-alkynyl nitroxide spinlabelling as a minimally perturbing method for probing DNA conformation.

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