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Spectrochim Acta A Mol Biomol Spectrosc ; 221: 117175, 2019 Oct 05.
Artigo em Inglês | MEDLINE | ID: mdl-31158770

RESUMO

As an effective lysosomal biomarker for oxidative stress status, cysteine (Cys) plays an important role in lysosomal proteolysis. Herein, we report the first lysosome-targetable fluorescence probe (MCAB) for Cys-selective detection based on nucleophilic addition reaction of sulfhydryl toward a α, ß-unsaturated ketone and demonstrate its application to lysosomal-targetable imaging. MCAB is designed based on a α, ß-unsaturated ethanoylcarbazole as the fluorophore and the thiols reaction site, and a methylcarbitol unit as a lysosome-targetable group. Upon reacting with Cys, this probe turns on highly specific fluorescence signals linearly proportional to Cys concentrations over the range of 0-300 µM. MCAB detects Cys with a rapid response time (within 12 min) and low limit of detection (0.38 µM). MCAB is highly selective to Cys over other similar biothiols including homocysteine (Hcy) and glutathione (GSH). Moreover, it also exhibits significant lysosomal-targetable ability, which is ideal for lysosomal Cys-selective imaging. Using MCAB, we have successfully visualized the fluctuation endogenous Cys in lysosomes under oxidative stress status in real-time.


Assuntos
Cisteína/análise , Corantes Fluorescentes/química , Lisossomos/metabolismo , Imagem Molecular/métodos , Estresse Oxidativo , Carbazóis/química , Linhagem Celular Tumoral , Corantes Fluorescentes/síntese química , Humanos , Peróxido de Hidrogênio/farmacologia , Concentração de Íons de Hidrogênio , Limite de Detecção , Lipopolissacarídeos/toxicidade , Lisossomos/efeitos dos fármacos , Microscopia de Fluorescência/instrumentação , Estresse Oxidativo/efeitos dos fármacos , Espectrometria de Fluorescência , Espectrofotometria Ultravioleta , Tempo
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