Electron transfer vs. proton transfer within radical-cation clusters of guanosine and deoxyguanosine with substituted naphthalenes and sinapinic acid

J Am Soc Mass Spectrom. 2001 Feb;12(2):176-9. doi: 10.1016/S1044-0305(00)00215-4.

Abstract

Guanosine (G) and deoxyguanosine (dG) radical cations can be generated in the gas phase by single electron transfer (SET) within nucleoside-dimethoxynaphthalenes (1-2) electron-bound heterodimers produced by fast atom bombardment in a four sector mass spectrometer. The nucleobase guanine is much more easily oxidized when it is linked to a ribose moiety. The radical cation dimers formed by G and dG with sinapinic acid behave as proton-bound heterodimers. The experiments mimic to some extent the migration of radical sites within stacking bases which causes DNA damaging through depurination processes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cations
  • Coumaric Acids / chemistry*
  • Coumaric Acids / radiation effects
  • Deoxyguanosine / chemistry*
  • Electron Transport
  • Guanosine / chemistry*
  • Hydrogen / chemistry
  • Naphthalenes / chemistry*
  • Naphthalenes / radiation effects
  • Spectrometry, Mass, Fast Atom Bombardment
  • Ultraviolet Rays

Substances

  • Cations
  • Coumaric Acids
  • Naphthalenes
  • Guanosine
  • sinapinic acid
  • Hydrogen
  • Deoxyguanosine