Fluorescent labelling: Difference between revisions
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'''Fluorescent |
'''Fluorescent labelling''' is the process of covalently attaching a [[fluorophore]] to another molecule, such as a [[protein]] or [[nucleic acid]]. This is generally accomplished using a [[reactive]] derivative of the fluorophore that selectively binds to a [[functional group]] contained in the target molecule. The most commonly labelled molecules are antibodies, which are then used as specific probes for detection of a particular target. |
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==Detection== |
==Detection== |
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==Labelling techniques== |
==Labelling techniques== |
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Fluorescent labelling is accomplished using a chemically reactive derivative of a fluorophore. Common reactive groups include amine reactive [[isothiocyanate]] derivatives such as [[FITC]] and [[TRITC]] (derivatives of [[fluorescein]] and [[rhodamine]]), amine reactive succinimidyl esters such as NHS-fluorescein, and [[sulfhydryl]] reactive [[maleimide]] activated fluors such as fluorescein-5-maleimide. Reaction of any of these reactive dyes with another molecule results in a stable [[covalent bond]] formed between a fluorophore and a labelled molecule. |
Fluorescent labelling is accomplished using a chemically reactive derivative of a fluorophore. Common reactive groups include amine reactive [[isothiocyanate]] derivatives such as [[FITC]] and [[TRITC]] (derivatives of [[fluorescein]] and [[rhodamine]]), amine reactive succinimidyl esters such as NHS-fluorescein, and [[sulfhydryl]] reactive [[maleimide]] activated fluors such as fluorescein-5-maleimide. Reaction of any of these reactive dyes with another molecule results in a stable [[covalent bond]] formed between a fluorophore and a labelled molecule. |
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Following a fluorescent labelling reaction, it is often necessary to remove any nonreacted fluorophore from the labelled target molecule. This is often accomplished by [[size exclusion chromatography]], taking advantage of the size difference between fluorophore and labelled protein, nucleic acid, etc. Fluorophores may interact with the separation matrix and reduce the effiency of separation. For this reason, specialized dye removal columns that account for the hydrophobic properties of fluorescent dyes are sometimes used. |
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Reactive fluorescent dyes are available from many sources (see below). They can be obtained with different reactive groups for attachment to various functional groups within the target molecule. They are also available in labelling kits that contain all the components to carry out a labelling reaction. |
Reactive fluorescent dyes are available from many sources (see below). They can be obtained with different reactive groups for attachment to various functional groups within the target molecule. They are also available in labelling kits that contain all the components to carry out a labelling reaction. |
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Revision as of 17:35, 7 November 2007
Fluorescent labelling is the process of covalently attaching a fluorophore to another molecule, such as a protein or nucleic acid. This is generally accomplished using a reactive derivative of the fluorophore that selectively binds to a functional group contained in the target molecule. The most commonly labelled molecules are antibodies, which are then used as specific probes for detection of a particular target.
Detection
Fluorescent labels are generally used for detection of a protein or other labelled molecule via a fluorescence microscope, flow cytometer or some other fluorescence reading instrument. These can be useful in localization of a target within a cell, flow cytometry (FACS) analysis, western blot assays, and other immunoanalytical methods.
Labelling techniques
Fluorescent labelling is accomplished using a chemically reactive derivative of a fluorophore. Common reactive groups include amine reactive isothiocyanate derivatives such as FITC and TRITC (derivatives of fluorescein and rhodamine), amine reactive succinimidyl esters such as NHS-fluorescein, and sulfhydryl reactive maleimide activated fluors such as fluorescein-5-maleimide. Reaction of any of these reactive dyes with another molecule results in a stable covalent bond formed between a fluorophore and a labelled molecule.
Following a fluorescent labelling reaction, it is often necessary to remove any nonreacted fluorophore from the labelled target molecule. This is often accomplished by size exclusion chromatography, taking advantage of the size difference between fluorophore and labelled protein, nucleic acid, etc. Fluorophores may interact with the separation matrix and reduce the effiency of separation. For this reason, specialized dye removal columns that account for the hydrophobic properties of fluorescent dyes are sometimes used.
Reactive fluorescent dyes are available from many sources (see below). They can be obtained with different reactive groups for attachment to various functional groups within the target molecule. They are also available in labelling kits that contain all the components to carry out a labelling reaction.