Two-photon excitation improves multifocal structured illumination microscopy in thick scattering tissue

Proc Natl Acad Sci U S A. 2014 Apr 8;111(14):5254-9. doi: 10.1073/pnas.1314447111. Epub 2014 Mar 24.

Abstract

Multifocal structured illumination microscopy (MSIM) provides a twofold resolution enhancement beyond the diffraction limit at sample depths up to 50 µm, but scattered and out-of-focus light in thick samples degrades MSIM performance. Here we implement MSIM with a microlens array to enable efficient two-photon excitation. Two-photon MSIM gives resolution-doubled images with better sectioning and contrast in thick scattering samples such as Caenorhabditis elegans embryos, Drosophila melanogaster larval salivary glands, and mouse liver tissue.

Keywords: multiphoton; superresolution.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology
  • Drosophila melanogaster / growth & development
  • Larva / chemistry
  • Lighting*
  • Liver / chemistry
  • Mice
  • Microscopy / methods*
  • Photons*