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Ellisman/AAAS' [8 j, O) Q3 J1 O. d3 ^ |
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New dyes developed by Guido Gaietta, Roger Tsien, Mark Ellisman (University of California at San Diego, La Jolla, CA), and colleagues allow efficient fluorescent and electron microscopy for studying the location, trafficking, assembly, and turnover of proteins and protein complexes."We were interested in being able to go from light microscopy to the EM level," says Ellisman. "In particular, we wanted better resolution than with immunogold labeling." To do so, the group examined FlAsH, a biarsenical derivative of fluorescein. FlAsH binds to small amino acid extensions containing the sequence C-C-X-X-C-C, which can be added to recombinant target proteins. Binding of FlAsH causes the ligand to emit a strong green fluorescence, and binding of ReAsH, a red variant, leads to red fluorescence.
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ReAsH is the variant that is useful for EM, because it can generate singlet oxygen upon illumination. Singlet oxygen drives localized polymerization of the substrate diaminobenzidene (DAB) into an insoluble form that can be viewed by EM. "Because the fluorescent label binds directly to the protein you are trying to localize, and the DAB polymer deposits directly nearby the fluorophore, the resolution is better ," says Ellisman. Additionally, this technique does not require the diffusion of large antibodies into the fixed specimens." E7 s) o8 U8 K M
0 M5 ^& ^3 ~0 W s0 k4 X0 EThe group put their new label to work by examining the protein connexin43, which multimerizes to form gap junctions. Pulse-chase with first FlAsH and then ReAsH revealed newer (i.e., red) molecules of connexin at the outer edge of large clusters of gap junctions known as plaques. Green molecules were concentrated in the center, indicating that older connexins are endocytosed from the middle of the plaques. EM demonstrated that newly synthesized connexins were first sent to nonplaque sites on the cell surface before flowing to the edge of a plaque.. U! A Z5 B8 X/ E& ]/ I
2 J$ z1 I' z+ R' P) V8 d& A( jThe team expects there will be many uses for the FlAsH-ReAsH system, especially in revealing how large complexes, such as receptor patches at synapses, are formed. "Anyone who has a question about how a cell manages the assembly of large macromolecular structures of a protein should benefit from the use of this system," says Ellisman.8 b9 b( _0 V9 s6 ~; H3 i! {
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Reference:
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Gaietta, G., et al. 2002. Science. 296:503–507.(New connexin (red) is added to the outsi) |
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发表于 2009-3-6 00:13
发表于 2015-5-25 17:27
