Time-resolved fluorescence spectroscopy and imaging of DNA labeled with DAPI and Hoechst 33342 using three-photon excitation

Biophys J. 1997 Feb;72(2 Pt 1):567-78. doi: 10.1016/s0006-3495(97)78696-x.

Abstract

We examined the fluorescence spectral properties of the DNA stains DAPI (4',6-diamidino-2-phenylindole, hydrochloride) and Hoechst 33342 (bis-benzimide, or 2,5'-bi'1H-benzimidazole2'-(4-ethoxyphenyl)-5-(4-methyl-1-piperazi nyl)) with two-photon (2h nu) and three-photon (3h nu) excitation using femtosecond pulses from a Ti:sapphire laser from 830 to 885 nm. The mode of excitation of DAPI bound to DNA changed from two-photon at 830 nm to three-photon at 885 nm. In contrast, Hoechst 33342 displayed only two-photon excitation from 830 to 885 nm. DAPI-DNA displayed the same emission spectra and decay times for 2h nu and 3h nu excitation. Hoechst 33342-DNA displayed the same intensity decay for excitation at 830 and 885 nm. Both probes displayed higher anisotropies for multiphoton excitation as compared to one-photon excitation with ultraviolet wavelengths, and DAPI-DNA displays a higher anisotropy for 3h nu at 885 nm than for 2h nu at 830 nm. We used 970-nm excitation of DAPI-stained chromosomes to obtain the first three-dimensional images with three-photon excitation. Three-photon excitation of DAPI-stained chromosomes at 970 nm was demonstrated by the power dependence in the fluorescence microscope.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Benzimidazoles*
  • Chemical Phenomena
  • Chemistry, Physical
  • Chromosomes
  • DNA / chemistry*
  • Fluorescence Polarization
  • Fluorescent Dyes*
  • HeLa Cells
  • Humans
  • Image Processing, Computer-Assisted
  • Indoles*
  • Kinetics
  • Lasers
  • Light
  • Metaphase
  • Microscopy, Fluorescence
  • Photons
  • Spectrometry, Fluorescence*
  • Spectrophotometry

Substances

  • Benzimidazoles
  • Fluorescent Dyes
  • Indoles
  • DAPI
  • DNA
  • bisbenzimide ethoxide trihydrochloride