Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo

被引:63
作者
Andersen, Kristen A. [1 ]
Aronoff, Matthew R. [2 ]
McGrath, Nicholas A. [2 ]
Raines, Ronald T. [2 ,3 ]
机构
[1] Univ Wisconsin, Mol & Cellular Pharmacol Grad Training Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
关键词
1,3-DIPOLAR CYCLOADDITIONS; BIOORTHOGONAL CHEMISTRY; TERMINAL ALKYNES; CLICK CHEMISTRY; LIVING CELLS; AZIDES; BIOSYNTHESIS; DIAZOMETHANE; GLYCANS; WATER;
D O I
10.1021/ja5095815
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We introduce a stabilized diazo group as a reporter for chemical biology. ManDiaz, which is a diazo derivative of N-acetylmannosamine, is found to endure cellular metabolism and label the surface of a mammalian cell. There its diazo group can undergo a 1,3-dipolar cycloaddition with a strained alkyne, providing a signal comparable to that from the azido congener, ManNAz. The chemoselectivity of diazo and alkynyl groups enables dual labeling of cells that is not possible with azido and alkynyl groups. Thus, the diazo group, which is approximately half the size of an azido group, provides unique opportunities for orthogonal labeling of cellular components.
引用
收藏
页码:2412 / 2415
页数:4
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