A Strategy for the Selective Imaging of Glycans Using Caged Metabolic Precursors

被引:76
作者
Chang, Pamela V.
Dube, Danielle H.
Sletten, Ellen M.
Bertozzi, Carolyn R. [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
PROSTATE-SPECIFIC ANTIGEN; FREE CLICK CHEMISTRY; LIVING ANIMALS; TUMOR-ANTIGENS; IMMUNOHISTOCHEMISTRY; ACTIVATION; TARGETS; PRODRUG; PROBES; PSA;
D O I
10.1021/ja101080y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Glycans can be imaged by metabolic labeling with azidosugars followed by chemical reaction with imaging probes; however, tissue-specific labeling is difficult to achieve. Here we describe a strategy for the use of a caged metabolic precursor that is activated for cellular metabolism by enzymatic cleavage. An N-azidoacetylmannosamine derivative caged with a peptide substrate for the prostate-specific antigen (PSA) protease was converted to cell-surface azido sialic acids in a PSA-dependent manner. The approach has applications in tissue-selective imaging of glycans for clinical and basic research purposes.
引用
收藏
页码:9516 / 9518
页数:3
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