Functional Imaging of Legumain in Cancer Using a New Quenched Activity-Based Probe

被引:139
作者
Edgington, Laura E. [1 ,2 ]
Verdoes, Martijn [2 ]
Ortega, Alberto [2 ]
Withana, Nimali P. [2 ]
Lee, Jiyoun [2 ]
Syed, Salahuddin [2 ]
Bachmann, Michael H. [3 ]
Blum, Galia [2 ]
Bogyo, Matthew [1 ,2 ,4 ]
机构
[1] Stanford Sch Med, Canc Biol Program, Stanford, CA 94305 USA
[2] Stanford Sch Med, Dept Pathol, Stanford, CA 94305 USA
[3] Stanford Sch Med, Dept Pediat, Stanford, CA 94305 USA
[4] Stanford Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
ANTIGEN PRESENTATION; CLASS-II; ASPARAGINE ENDOPEPTIDASE; PROTEASE ACTIVITY; EXPRESSION; DEGRADATION; TARGET; GROWTH;
D O I
10.1021/ja307083b
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Legumain is a lysosomal cysteine protease whose biological function remains poorly defined. Legumain activity is up-regulated in most human cancers and inflammatory diseases most likely as the result of high expression in populations of activated macrophages. Within the tumor microenvironment, legumain activity is thought to promote tumorigenesis. To obtain a greater understanding of the role of legumain activity during cancer progression and inflammation, we developed an activity-based probe that becomes fluorescent only upon binding active legumain. This probe is highly selective for legumain, even in the context of whole cells and tissues, and is also a more effective label of legumain than previously reported probes. Here we present the synthesis and application of our probe to the analysis of legumain activity in primary macrophages and in two mouse models of cancer. We find that legumain activity is highly correlated with macrophage activation and furthermore that it is an ideal marker for primary tumor inflammation and early stage metastatic lesions.
引用
收藏
页码:174 / 182
页数:9
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