Development of fluorescent probes based on protection-deprotection of the key functional groups for biological imaging

被引:380
作者
Tang, Yonghe [1 ]
Lee, Dayoung [2 ]
Wang, Jiaoliang [3 ]
Li, Guanhan [1 ]
Yu, Jinghua [1 ]
Lin, Weiying [1 ,3 ]
Yoon, Juyoung [2 ]
机构
[1] Univ Jinan, Sch Biol Sci & Technol, Sch Chem & Chem Engn, Inst Fluorescent Probes Biol Imaging, Jinan 250022, Shandong, Peoples R China
[2] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 120750, South Korea
[3] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemobiosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
新加坡国家研究基金会;
关键词
SE-N BOND; TURN-ON; HYDROGEN-PEROXIDE; LIVING CELLS; COLORIMETRIC CHEMOSENSORS; RATIOMETRIC DETECTION; THIOLS; HYDRAZINE; FLUORIDE; CYSTEINE;
D O I
10.1039/c5cs00103j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, the strategy of protection-deprotection of functional groups has been widely employed to design fluorescent probes, as the protection-deprotection of functional groups often induces a marked change in electronic properties. Significant advances have been made in the development of analyte-responsive fluorescent probes based on the protection-deprotection strategy. In this tutorial review, we highlight the representative examples of small-molecule based fluorescent probes for bioimaging, which are operated via the protection-deprotection of key functional groups such as aldehyde, hydroxyl, and amino functional groups reported from 2010 to 2014. The discussion includes the general protection-deprotection methods for aldehyde, hydroxyl, or amino groups, as well as the design strategies, sensing mechanisms, and deprotection modes of the representative fluorescent imaging probes applied to bio-imaging.
引用
收藏
页码:5003 / 5015
页数:13
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