Team:Slovenia/PROJECT/proof/popfret/back

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Revision as of 15:28, 27 October 2010

Chuck Norris facts:




A green fluorescent protein (GFP), first isolated in the 60s from a jellyfish Aequorea victoria, has been mutated in many different ways leading to a wide variety of fluorescent proteins with novel fluorescent properties.

San Diego beach scene drawn with an eight color palette of bacterial colonies expressing fluorescent proteins derived from GFP and the red-fluorescent coral protein dsRed. (Roger Y. Tsien, Nobel Lecture 2008)

It has been shown (Segal et al., 2005), that after splitting a fluorescent protein in two parts and fusing them with DNA specific binding domains, they can be brought together by the addition of a DNA containing specific DNA binding motifs for both DNA binding domains, leading to reconstitution and maturation of a functional fluorescent protein. It has also been reported than an amino acid overlap at the stitching point of split protein accelerates and enhances protein reassembly (Kerppola et al., 2003). We further developed this concept by testing split GFP reconstitution on a DNA program sequence leading to FRET effect in vivo thereby proving sequential binding of as much as four DNA binding factors on a predefined DNA program.

FRET (Förster resonance energy transfer) is a well known physical phenomena describing non-radiative energy transfer between two fluorophores. For FRET to occur two conditions have to be fullfield. Firstly, fluorophores must have overlapping fluorescence emission (donor fluorophore) and excitation (acceptor fluorophore) spectra and secondly, donor and acceptor fluorophore have to be close enough, meaning at angstrom range, so that non-radiative energy transfer can occur. Many suitable pairs among fluorescent proteins can be found that are convenient for FRET experiments. mCerulean and mCitrine are two among them being especially suitable for FRET studies.

This phenomena is used in a variety of molecular biology techniques, mainly for studying protein-protein interactions since FRET is a function of distance separating fluorescent proteins. This dependance can be simply illustrated as follows: if you double the distance between donor and acceptor molecule, FRET efficiency will be 64-times lower. This relationship is exactly represented as follows:

Be2895beaa166bf3d13d1ae09406dace.png

where E represents the fraction of energy transfer per donor excitation event, r is the distance between donor and acceptor molecule and R0Förster distance (the distance at which FRET efficiency between two adjacent molecules is 50%).

In our experiments we used a following FRET pair: mCerulean (CFP) and mCitrine (YFP). The donor, CFP, was excited with a 458-nm Argon laser and detected at 470–500 nm. An acceptor, YFP, was excited with a 514-nm Argon laser and detected at 520 to 580 nm window. The emission spectra of donor CFP overlaps with the acceptor YFP excitation spectra, which is sufficient for FRET when both fluorophores are close to each other. The FRET is detected as light emitted from acceptor only when donor was excited first. An acceptor photobleaching is used to confirm that we observe the FRET effect in cells. The de-quenching of the donor upon photo-destructing the acceptor results in an increase of the donor fluorescence, which is proportional to the FRET efficiency E.