Pereira da Silva Neves Marta Maria, González-García María Begoña, Pérez-Junquera Alejandro, Hernández-Santos David, Fanjul-Bolado Pablo
DropSens S.L, Ed. CEEI, Parque Tecnológico de Asturias, Llanera, Asturias, Spain.
Luminescence. 2018 May;33(3):552-558. doi: 10.1002/bio.3445. Epub 2018 Jan 21.
In this work, a turn-off photoluminescent sensing proof-of-concept based on blue luminescent graphene quantum dots (GQDs) as the fluorescent probe was developed. For that purpose, GQDs optical response was related with the catalytic enzymatic activity of alkaline phosphatase (ALP), in the presence of hydroquinone diphosphate (HQDP). The hydrolysis of HQDP by ALP generated hydroquinone (HQ). The oxidation of HQ, enzymatically produced, to p-benzoquinone (BQ) resulted in the quenching of GQDs fluorescence (FL). Therefore, the developed luminescent sensing mechanism allowed the FL quenching with ALP activity to be related and thus quantified the concentration of ALP down to 0.5 nM of enzyme. This innovative design principle appears as a promising tool for the development of enzymatic sensors based on ALP labeling with fluorescent detection or even for direct ALP luminescent quantification in an easy, fast and sensitive manner.
在这项工作中,基于蓝色发光石墨烯量子点(GQDs)作为荧光探针,开发了一种基于光致发光关闭的传感概念验证。为此,在对苯二酚二磷酸(HQDP)存在的情况下,将GQDs的光学响应与碱性磷酸酶(ALP)的催化酶活性相关联。ALP对HQDP的水解产生对苯二酚(HQ)。酶促产生的HQ氧化为对苯醌(BQ)导致GQDs荧光(FL)猝灭。因此,所开发的发光传感机制使得FL猝灭与ALP活性相关,从而能够将ALP浓度定量至低至0.5 nM的酶。这种创新的设计原理似乎是一种很有前景的工具,可用于开发基于荧光检测的ALP标记的酶传感器,甚至以简单、快速和灵敏的方式直接进行ALP发光定量。