Resumen
cDNA encoding VEGF and Ig-like extracellular domains 2-4 of VEGFR-1 (sFlt-12-4) were cloned into prokaryotic expression vectors pET32a and pQE60. Recombinant proteins were purified (metal affinity chromatography) and renatured. Chemiluminescent study for the interaction of recombinant VEGF and sFlt-12-4 showed that biotinylated VEGF specifically binds to the polystyrene-immobilized receptor extracellular fragment. Biotinylated recombinant sFlt-1 interacts with immobilized VEGF. Analysis of the interaction of immobilized recombinant VEGFR-1 and VEGF with C6 glioma cells labeled with CFDA-SE (vital fluorescent dye) showed that recombinant VEGFR-1 also binds to native membrane-associated VEGF. Recombinant VEGF was shown to bind to specific receptors expressed on the surface of C6 glioma cells. Functional activity of these proteins was confirmed by ligand-receptor assay for VEGF and VEGFR-1 (sFlt-1) and quantitative chemiluminescent detection.
| Idioma original | English (US) |
|---|---|
| Páginas (desde-hasta) | 707-711 |
| Número de páginas | 5 |
| Publicación | Bulletin of Experimental Biology and Medicine |
| Volumen | 152 |
| N.º | 6 |
| DOI | |
| Estado | Published - abr 2012 |
| Publicado de forma externa | Sí |
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology
Huella
Profundice en los temas de investigación de 'Ligand-receptor assay for evaluation of functional activity of human recombinant VEGF and VEGFR-1 extracellular fragment'. En conjunto forman una huella única.Citar esto
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