A lysosome-targetable and two-photon fluorescent probe for imaging endogenous β-galactosidase in living ovarian cancer cells

被引:61
作者
Huang, Jinxin [1 ]
Li, Nan [1 ]
Wang, Qianqian [1 ]
Gu, Yueqing [1 ,2 ]
Wang, Peng [1 ]
机构
[1] China Pharmaceut Univ, Sch Engn, Dept Biomed Engn, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Two-photon; Fluorescent probe; beta-gal; Lysosomal targeting; TUMORS;
D O I
10.1016/j.snb.2017.02.158
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The early diagnosis of ovarian cancer plays an important role in the treatment of ovarian cancer. beta-Galactosidase(beta-gal) which is an overexpressed enzyme in primary ovarian cancer can be employed as a valuable biomarker of ovarian cancer. A fluorescent probe for beta-gal detection and imaging is of important significance for the diagnosis of primary ovarian cancer. Toward this goal, we have rationally designed and synthesized a novel two-photon fluorescence probe FC-beta gal for monitoring endogenous,beta-gal in lysosome. The probe FC-beta gal showed apparently fluorescence changes from blue to green in response to beta-gal by the cleavage of glycosidic bond. 4-Propylmorpholine group endowed the probe with the property of lysosomal targeting. We confirmed that the probe FC-beta gal exhibited rapid response, high sensitivity, excellent biocompatibility and favorable performances to beta-gal even in the interfering of other biologic substances. In addition, single photon and two-photon confocal imaging experiments indicated that probe FC-beta gal displayed a desirable cellular imaging for endogenous beta-gal in human ovarian cancer SKOV-3 cells with low cytotoxicity. Moreover, the probe had satisfactory ability to accumulate into lysosomes compared with LysoTracker. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:833 / 839
页数:7
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