Exonucleolytic degradation of high-density labeled DNA studied by fluorescence correlation spectroscopy

Analyst. 2012 Mar 7;137(5):1160-7. doi: 10.1039/c2an15879e. Epub 2012 Jan 23.

Abstract

The exonucleolytic degradation of high-density labeled DNA by exonuclease III was monitored using two-color fluorescence correlation spectroscopy (FCS). One strand of the double stranded template DNA was labeled on either one or two base types and additionally at one end via a 5' Cy5 tagged primer. Exonucleolytic degradation was followed via the diffusion time, the brightness of the remaining DNA as well as the concentration of released labeled bases. We found a hydrolyzation rate of about 11 to 17 nucleotides per minute per enzyme (nt/min/enzyme) for high-density labeled DNA, which is by a factor of about 4 slower than for unlabeled DNA. The exonucleolytic degradation of a 488 base pair long double stranded DNA resulted in a short double stranded DNA segment of 112 ± 40 base pairs (bp) length with two single-stranded tails.

MeSH terms

  • Color
  • DNA / chemistry
  • DNA / metabolism*
  • Diffusion
  • Exodeoxyribonucleases / metabolism
  • Fluorescent Dyes / chemistry
  • Kinetics
  • Spectrometry, Fluorescence / methods*
  • Staining and Labeling

Substances

  • Fluorescent Dyes
  • DNA
  • Exodeoxyribonucleases
  • exodeoxyribonuclease III