Abstract
We demonstrate broad-field, non-scanning, two-photon excitation fluorescence (2PEF) close to a glass/cell interface by total internal reflection of a femtosecond-pulsed infrared laser beam. We exploit the quadratic intensity dependence of 2PEF to provide non-linear evanescent wave (EW) excitation in a well-defined sample volume and to eliminate scattered background excitation. A simple model is shown to describe the resulting 2PEF intensity and to predict the effective excitation volume in terms of easily measurable beam, objective and interface properties. We demonstrate non-linear evanescent wave excitation at 860 nm of acridine orange-labelled secretory granules in live chromaffin cells, and excitation at 900 nm of TRITC-phalloidin-actin/GPI-GFP double-labelled fibroblasts. The confined excitation volume and the possibility of simultaneous multi-colour excitation of several fluorophores make EW 2PEF particularly advantageous for quantitative microscopy, imaging biochemistry inside live cells, or biosensing and screening applications in miniature high-density multi-well plates.
MeSH Terms
Animals
Cattle
Chromaffin Cells/cytology,metabolism
Computer Simulation
Cytoskeleton/metabolism,ultrastructure
Equipment Design
Equipment Failure Analysis
Mice
Microscopy, Fluorescence, Multiphoton/methods
Models, Biological
Reproducibility of Results
Secretory Vesicles/metabolism,ultrastructure
Sensitivity and Specificity
Swiss 3T3 Cells
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schapper Florian
Neurophysiology and New Microscopies, Ecole Supérieure de Physique et Chimie Industrielles (ESPCI), 10 rue Vauquelin, 75005 Paris, France.
Gonçalves José Tiago
Oheim Martin
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