Pregled bibliografske jedinice broj: 838679
How to track active Rac1 in live Dictyostelium cells?
How to track active Rac1 in live Dictyostelium cells? // International Meeting of the German Society for Cell Biology
München, 2016. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 838679 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
How to track active Rac1 in live Dictyostelium cells?
Autori
Marinović, Maja ; Šoštar, Marko ; Filić Vedrana, Antolović, Vlatka ; Weber Igor
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
International Meeting of the German Society for Cell Biology
/ - München, 2016
Skup
International Meeting of the German Society for Cell Biology
Mjesto i datum
München, Njemačka, 14.03.2016. - 16.03.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Dictyostelium discoideum; Rac1; biosensor
Sažetak
Small Rho GTPases are major regulators of the actin cytoskeleton dynamics in eukaryotic cells. Common approaches for examination of their activity in living cells include probes based on fluorescence resonance energy transfer (FRET), bimolecular fluorescence complementation (BiFC) and photoactivation. However, these methods might be of limited use, because short time available for image acquisition often leads to a low signal-to-noise ratio. Attempts to overcome this effect by increasing the intensity of illumination are restricted by photobleaching of probes and the cell’s photosensitivity. Here, we describe characterization of a new fluorescent probe that selectively binds to active forms of Dictyostelium Rac1 GTPases, and demonstrate its superior properties for live cell imaging. The probe is based on the GTPase-binding domain (GBD) from DPAKa kinase, and was selected on the basis of yeast two-hybrid screen, GST pull-down assay, and FRET measurements by fluorescence lifetime imaging microscopy (FLIM). It binds specifically to active Rac1 which is located at the cell membrane and has a low cytoplasmic background. Overexpression of DPAKa(GBD)-DYFP probe induces no adverse effects on cell motility as estimated by a quantitative cell migration assay. In the end, its finely tuned intensity distribution enables quantitative measurements of the Rac1 activity in different parts of the cell membrane.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb