Advances in Activity-Based Sensing Probes for Isoform-Selective Imaging of Enzymatic Activity

被引:58
作者
Gardner, Sarah H. [2 ]
Reinhardt, Christopher J. [1 ]
Chan, Jefferson [1 ,2 ]
机构
[1] Univ Illinois, Beckman Inst Adv Sci & Technol, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
activity-based sensing; fluorescence; molecular imaging; probe development; rational design; RATIOMETRIC FLUORESCENT-PROBE; ALDEHYDE DEHYDROGENASE 1A1; HUMAN CARBOXYLESTERASE 2; NUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE; CYTOCHROME-P450; MECHANISM; ENZYMES; CYCLOOXYGENASE-2; PHOSPHATASES; CANCER;
D O I
10.1002/anie.202003687
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Until recently, there were no generalizable methods for assessing the effects of post-translational regulation on enzymatic activity. Activity-based sensing (ABS) has emerged as a powerful approach for monitoring small-molecule and enzyme activities within living systems. Initial examples of ABS were applied for measuring general enzymatic activity; however, a recent focus has been placed on increasing the selectivity to monitor a single enzyme or isoform. The highest degree of selectivity is required for differentiating between isoforms, where the targets display significant structural similarities as a result of a gene duplication or alternative splicing. This Minireview highlights key examples of small-molecule isoform-selective probes with a focus on the relevance of isoform differentiation, design strategies to achieve selectivity, and applications in basic biology or in the clinic.
引用
收藏
页码:5000 / 5009
页数:10
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