Near-infrared fluorescent probes for peptidases

被引:78
|
作者
Chin, Jik [1 ]
Kim, Hae-Jo [2 ]
机构
[1] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
[2] Hankuk Univ Foreign Studies, Dept Chem, Yongin 17035, South Korea
基金
新加坡国家研究基金会;
关键词
Aminopeptidase; Enzyme targeting; Glutamyltranspeptidase; Near-infrared fluorophore; Penicillin amidase; Protease; GAMMA-GLUTAMYL-TRANSPEPTIDASE; LEUCINE AMINOPEPTIDASE ACTIVITY; SQUARAINE-DERIVED ROTAXANES; ACTIVATABLE OPTICAL PROBES; INDUCED LIVER-INJURY; IN-VIVO; CYSTEINE CATHEPSINS; PHOTODYNAMIC THERAPY; SELECTIVE DETECTION; NIR FLUORESCENCE;
D O I
10.1016/j.ccr.2017.07.009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Near-infrared (NIR) fluorescent probes possess a characteristic molecular structure with a highly conjugated polyene or polynuclear system, thus exhibiting a long emission wavelength over 650 nm up to 900 nm. They are of increasing interest owing to their capability of deep tissue penetration as well as low spectral interference with biomolecules in the living system. In this review, we will examine typical molecular structures of NIR fluorophores and then describe their enzymatic reactions with peptidases from the viewpoint of chemical design and reaction mechanism. The targeting enzymes will be covered from aminopeptidase, glutamyltranspeptidase, protease to penicillin G-amidase. Further application to tumor imaging and therapy is also discussed as a theranostic approach. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 181
页数:13
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