A Self-Assembling Probe for Imaging the States of Golgi Apparatus in Live Single Cells

被引:8
|
作者
Tan, Weiyi [1 ]
Zhang, Qiuxin [1 ]
Hong, Pengyu [2 ]
Xu, Bing [1 ]
机构
[1] Brandeis Univ, Dept Chem, Waltham, MA 02454 USA
[2] Brandeis Univ, Dept Comp Sci, Waltham, MA 02453 USA
关键词
TRANSPORT; ER;
D O I
10.1021/acs.bioconjchem.2c00084
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Despite the enormous progress in genomics and proteomics, it is still challenging to assess the states of organelles in living cells with high spatiotemporal resolution. Based on our recent finding of enzyme-instructed self-assembly of a thiophosphopeptide that targets the Golgi Apparatus (GA) instantly, we use the thiophosphopeptide, which is enzymatically responsive and redox active, as an integrative probe for revealing the state of the GA of live cells at the single cell level. By imaging the probe in the GA of live cells over time, our results show that the accumulation of the probe at the GA depends on cell types. By comparison to a conventional Golgi probe, this self-assembling probe accumulates at the GA much faster and are sensitive to the expression of alkaline phosphatases. In addition, subtle changes of the fluorophore results in slightly different GA responses. This work illustrates a novel class of active molecular probes that combine enzyme-instructed self assembly and redox reaction for high-resolution imaging of the states of subcellular organelles over a large area and extended times.
引用
收藏
页码:1983 / 1988
页数:6
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