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ACS Chem Biol ; 9(10): 2359-65, 2014 Oct 17.
Artigo em Inglês | MEDLINE | ID: mdl-25105835

RESUMO

One major limitation of labeling proteins with synthetic fluorophores is the high fluorescence background, which necessitates extensive washing steps to remove unreacted fluorophores. In this paper, we describe a novel fluorogenic probe based on an environment-sensitive fluorophore for labeling with SNAP-tag proteins. The probe exhibits dramatic fluorescence turn-on of 280-fold upon being labeled to SNAP-tag. The major advantages of our fluorogenic probe are the dramatic fluorescence turn-on, ease of synthesis, high selectivity, and rapid labeling with SNAP-tag. No-wash labeling of both intracellular and cell surface proteins was successfully achieved in living cells, and the localization of these proteins was specifically visualized.


Assuntos
Citosol/metabolismo , Corantes Fluorescentes/química , Imagem Molecular/métodos , Sondas Moleculares , Proteínas/metabolismo , Citometria de Fluxo , Células HCT116 , Humanos
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