Data di Pubblicazione:
2015
Abstract:
We report the rational design, based on docking simulations, and
synthesis of the first fluorescent and selective probe of GPER for
bioimaging purposes and functional dissecting studies. It has been
conceived as a Bodipy derivative and obtained by accessible and
direct synthesis. Its optical properties have been measured in
different solvents, showing insensitivity to their polarity. Its
binding to GPER was achieved by competition assays with [3H]E2
and [5,6-3H] nicotinic acid in ER-negative and GPER-positive SkBr3
breast cancer cells. SkBr3 cells, transfected with a GPER expression
vector containing a FLAG tag, were used to confirm that the
fluorophore binds to GPER in a specific manner.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
synthesis, BODIPY, GPER
Elenco autori:
Papalia, Teresa; Lappano, R.; Barattucci, Anna; Pisano, A.; Bruno, Giuseppe; Santolla, M. F.; Campagna, Sebastiano; De Marco, P.; Puntoriero, Fausto; De Francesco, E. M.; Rosano, C.; Maggiolini, M.; Bonaccorsi, Paola Maria
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