Bio-orthogonal Click Chemistry for In Vivo Bioimaging

被引:90
|
作者
Kenry [1 ]
Liu, Bin [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117585, Singapore
来源
TRENDS IN CHEMISTRY | 2019年 / 1卷 / 08期
关键词
AZIDE-ALKYNE CYCLOADDITION; COPPER-FREE; BIOORTHOGONAL CHEMISTRY; STAUDINGER LIGATION; 1,3-DIPOLAR CYCLOADDITIONS; TERMINAL ALKYNES; SMALL MOLECULES; CANCER; GLYCOSYLATION; PROTEINS;
D O I
10.1016/j.trechm.2019.08.003
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rapid advancement of bio-orthogonal click chemistry in the past decade has enabled the study and precise manipulation of biological processes within living organisms. The capability to induce fast and selective chemical reactions between two exogenous complementary moieties in living systems, with negligible perturbation to their native activities, have rendered bio-orthogonal click chemistry highly promising for a multitude of bioapplications. This review provides an overview of recent developments in bio-orthogonal click chemistry for bioimaging in living organisms. Bio-orthogonal click reactions commonly performed in in vivo systems and their in vivo biological labeling and imaging applications, particularly for the visualization of bio-molecular processes, therapeutic cells, tumors, and bacteria, are discussed. Potential future directions of this exciting area are also presented.
引用
收藏
页码:763 / 778
页数:16
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