By Deborah Fields, BSc (Hons), PgDip, MCIPR
In fluorescence microscopy, a specimen emits energy when activated by light of a certain wavelength. Some substances such as chlorophyll and some minerals will do this naturally, while others will need the help of other chemical triggers.
Fluorescence microscope components
A fluorescence microscope is typically made up of the following components:
- A light source, which may be a xenon or mercury burner, an LED or a laser.
- An excitation filter, which selects from the light source only the excitation wavelengths that are able to excite the specimen.
- A dichroic beam splitter or mirror which transmits and reflects light as a function of wavelength.
- An emission filter, which ensures only light emitted from the sample is transmitted, by selecting for light of a distinct wavelength.
- A CCD camera, which is the most widely used device for detecting the emitted light. It is usually linked to a computer screen which displays the images generated
Modern microscope station with atibody-stained tissue sample image on the screen. Image Copyright: anyaivanova / Shutterstock
Types of fluorescence microscopy
The Greek word “epi” means the same. In epifluorescence microscopy, the illuminated and emitted light both travel through the same objective lens.
The light source is often a xenon or mercury burner, but more recently, LEDs have become popular. A filter is used to select wavelengths coming from the light source.
The light reaches the specimen via a microscope objective lens and is absorbed by the fluorophores. The emitted light from the sample travels back through the objective lens, towards the emission filter and detector.
Fibroblast cells with fluorescence microscopy Image Copyright: Heiti Paves / Shutterstock
Total internal reflection fluorescence (TIRF)
This technique ensures that the excitation light does not make it very far into the sample. For example, if neurons are placed in solution on a glass slide, some of them will stick to the surface of the glass.
In TIRF, the light is sent sideways into the slide, which means it does not get very far into the solution containing the specimen; it just leaks into the solution, but only very near to the glass surface.
Light is then only emitted in a very thin area against the surface of the glass. This can provide very clear images for a sample such as neurons, where a lot happens on the cell surface.
Here, a laser spot is focused in the same plane as the focus of the microscope. Light that is not from the microscope focus is blocked by a pinhole in front of the detector.
Ordinarily with epifluorescence, the microscope would collect all light within the microscope field of view, including light that is not from the microscope focus. This process means the out-of-focus light is blocked and does not reach the detector.
The arrangement of the objective, collection optics and pinhole in confocal microscopy has to be very precise for the microscope to work properly. Multiphoton fluorescence uses laser light of a wavelength that only has half the energy it needs to be in order to excite the sample.
Fluorophores in the sample will only become excited and emit light when the laser is bright enough for photons to reach the fluorophores very quickly, which only happens when the laser light is directed to a very small spot. Therefore, light is only emitted from the area of the sample where the laser is focused. This eradication of background light results in very clean, sharp images.
Structured illumination microscopy (SIM) and stimulated emission depletion microscopy both work by restricting the size of the spot that emits light by reducing the size of the excitation spot. This is because a focused spot of light can only cannot get any smaller than around 200nm and single molecules are much smaller than this.
Reviewed by Sally Robertson, BSc
Last Updated: Jun 14, 2016