Principle of Stimulated Emission Depletion (STED) Microscopy

Abstract

Stimulated Emission Depletion (STED) Microscopy describes a commonly used technique to achieve super resolution in biological applications. In this method two laser beams – one normal, one transformed into a donut-mode – are superimposed onto a fluorescent specimen. By using excitation and depletion of the fluorescent processes and exploiting the resulting saturation effects, the back reflected light exhibits a much higher resolution compared to usual microscopy techniques (e.g., widefield microscopy). In this document the basic setup of such a device is presented. For modeling the saturation effect, an equivalent aperture is applied in the focal region.

VirtualLab Fusion Configuration

  • VirtualLab Fusion VirtualLab Fusion

Are you interested in further reading?

Tutorial

Simulation of Multiple Light Sources with VirtualLab Fusion

This document illustrates how to use the Multiple Light Source in VirtualLab Fusion.

Use Case

Focusing of Gaussian-Laguerre Beam for STED Microscopy

It is demonstrated that the focusing of high order Gaussian-Laguerre beam generates donut-shaped PSF. The size of donut-shaped PSF can be adjusted by different high orders.