Axial nanoscale localization by normalized total internal reflection fluorescence microscopy

Opt Lett. 2014 Feb 15;39(4):869-72. doi: 10.1364/OL.39.000869.

Abstract

We present a simple modification of a standard total internal reflection fluorescence microscope to achieve nanometric axial resolution, typically ≈10 nm. The technique is based on a normalization of total internal reflection images by conventional epi-illumination images. We demonstrate the potential of our method to study the adhesion of phopholipid giant unilamellar vesicles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Membrane / metabolism
  • Image Processing, Computer-Assisted
  • Microscopy, Fluorescence / methods*
  • Unilamellar Liposomes / metabolism

Substances

  • Unilamellar Liposomes