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Fluorescence Microscopy

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Fluorescent molecules emit light when they are illuminated with light of a shorter wavelength. Familiar examples are the hidden signature in bank passbooks, whichis written in fluorescent ink that glows blue (wavelength about 450 nm) when illuminated with ultraviolet light (UV) (wavelength about 360 nm), and the whitener in fabric detergents that causes your white shirt to glow blue when illuminated by the ultraviolet light in a club. The fluorescent dye Hoechst 33342 has a similar wavelength dependence: It is excited by UV light and emits blue light. However, it differs from the dyes used in ink or detergent in that it binds tightly to the DNA in the nucleus and only fluoresces when so bound. Diagram a shows the optical path through a microscope set up so as to look at a preparation stained with Hoechst.



White light from an arc lamp passes through an excitation filter that allows only UV light to pass. This light then strikes the heart of the fluorescent microscope: a special mirror called a dichroic mirror that reflects light of wavelengths shorter than a designed cutoff but transmits light of longer wavelength. To view Hoechst, we use a dichroic mirror of cutoff wavelength 400 nm, which therefore reflects the UV excitation light up through the objective lens and onto the specimen. Any Hoechst bound to DNA in the preparation will emit blue light. 

Some of this will becaptured by the objective lens and, because its wavelength is greater than 400 nm, will not be reflected by the dichroic mirror but will instead pass through. An emission filter, set to pass only blue light, cuts out any scattered UV light. The blue light now passes to the eye or camera in the usual way. Image b shows a field of cells cultured from rat brain (gift of Dr. Charles Krieger, Simon Fraser University) after staining with Hoechst. Only the nuclei are seen, as bright ovals.

Although some of the structures and chemicals found in cells can be selectively stained by specific fluorescent dyes, others are most conveniently revealed by using antibodies. In this technique an animal (usually a mouse, rabbit, or goat) is injected with a protein or other chemical of interest. The animal’s immune system recognizes the chemical as foreign and generates antibodies that bind to (and therefore help neutralize) the chemical. Some blood is then taken from the animal and the antibodies purified. The antibodies can then be labeled by attaching a fluorescent dye. Images c and d show the same field of brain cells but with the excitation filter, dichroic mirror, and emission filter changed so as to reveal in c a protein called ELAV that is found only in nerve cells; then in d an intermediate filament protein (page 000) found only in glial cells. 

The antibody that binds to ELAV is labeled with a fluorescent dye that is excited by blue light and emits green light. The antibody that binds to the glial filaments is labeled with a dye that is excited by green light and emits red light. Because these wavelength characteristics are different, the location of the three chemicals—DNA, ELAV, and intermediate filament—can be revealed independently in the same specimen. See the CBASC website for an imageof all three signals in color and superimposed.


The technique just described is called primary immunofluorescence and requires that the antibody to the chemical of interest be labeled with a dye. Only antibodies to chemicals that many laboratories study are so labeled. In order to reveal other chemicals, scientists use secondary immunofluorescence. In this approach, a commercial company injects an animal (e.g., a goat) with an antibody from another animal (e.g., a rabbit). The goat then makes “goat anti rabbit” antibody. This, called the secondary antibody, is purified and labeled with a dye. All the scientist has to do is make or buy a rabbit antibody that binds to the chemical of interest. No further modification of this specialized, primary antibody is necessary.

Once the primary antibody has bound to the specimen and excess antibody rinsed off, the specimen is then exposed to the secondary antibody that binds selectively to the primary antibody. Viewing the stained preparation in a fluorescence microscope then reveals the location of the chemical of interest. The same dye-labeled secondary antibody can be used in other laboratories or at other times to reveal the location of many different chemicals because the specificity is determined by the unlabeled primary antibody.

source:

Bolsover, S. R., Hyams, J.,Shepard, E. (2004). Cell biology: a short course 2nd Ed. Hoboken: New 
                  Jersey. Willey and sons Inc. Publishing 
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Fluorescence Microscopy | Muhammad Luthfi Hidayat | 5

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