Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University , Xiangtan, 411105, People's Republic of China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University , Changsha, 410082, People's Republic of China.
Anal Chem. 2017 Jun 20;89(12):6854-6860. doi: 10.1021/acs.analchem.7b01351. Epub 2017 May 30.
Alkaline phosphatase (ALP) is an essential enzyme and widely distributes in a variety of tissues. To date, various nanomaterial and small-molecule fluorescent probes for ALP have been constructed successfully, but the emission wavelengths of these probes are in the ultraviolet or visible range, which is not beneficial for bioimaging. Herein, a hemicyanine-based near-infrared (NIR) fluorescent probe named CyP is first synthesized and used to detect ALP activity. The characteristics of probe CyP are as follows: (1) The probe possesses a facile structure, which can be obtained by easy synthetic steps. (2) The fluorescence emission of the sensing system is at 738 nm belonging to NIR region, which is suitable for bioimaging in vivo. (3) The probe exhibits high sensitivity to ALP with 10-fold fluorescence enhancement and low detection limit (0.003 U/mL) can match the level of ALP in vivo. (4) The fluorescent change of the probe is attributed to the fact that ALP-catalyzed cleavage of the phosphate group in CyP induces the transformation of CyP (fluorescence off) into CyOH (fluorescence on), which is proved by HPLC, P NMR, MS, and DFT calculation. (5) The NIR fluorescent probe is applied for the detection of endogenous ALP activity in various biological samples such as cell, tissue, and living animal with satisfactory results.
碱性磷酸酶(ALP)是一种重要的酶,广泛分布于多种组织中。迄今为止,已经成功构建了各种用于 ALP 的纳米材料和小分子荧光探针,但这些探针的发射波长在紫外或可见光范围内,不利于生物成像。在此,首次合成了一种基于半花菁的近红外(NIR)荧光探针 CyP,并用于检测 ALP 活性。探针 CyP 的特点如下:(1)探针具有简单的结构,可以通过简单的合成步骤获得。(2)传感系统的荧光发射位于 738nm 的近红外区域,适用于体内生物成像。(3)探针对 ALP 具有高灵敏度,荧光增强 10 倍,检测限低(0.003 U/mL),可与体内的 ALP 水平相匹配。(4)荧光变化归因于 ALP 催化裂解 CyP 中的磷酸基团,诱导 CyP(荧光关闭)转化为 CyOH(荧光打开),这一点通过 HPLC、P NMR、MS 和 DFT 计算得到了证实。(5)该 NIR 荧光探针已成功应用于各种生物样品(如细胞、组织和活体动物)中内源性 ALP 活性的检测,结果令人满意。