Imaging the glycome

被引:249
作者
Laughlin, Scott T. [1 ]
Bertozzi, Carolyn R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
azide; chemical reporter; click chemistry; glycan; bioorthogonal; O-LINKED GLYCOSYLATION; STAUDINGER LIGATION; IN-VIVO; MONOCLONAL-ANTIBODY; FLUORESCENT SENSOR; CELL-SURFACES; LIVING CELLS; CAENORHABDITIS-ELEGANS; N-ACETYLGLUCOSAMINE; TERMINAL ALKYNES;
D O I
10.1073/pnas.0811481106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular imaging enables visualization of specific molecules in vivo and without substantial perturbation to the target molecule's environment. Glycans are appealing targets for molecular imaging but are inaccessible with conventional approaches. Classic methods for monitoring glycans rely on molecular recognition with probe-bearing lectins or antibodies, but these techniques are not well suited to in vivo imaging. In an emerging strategy, glycans are imaged by metabolic labeling with chemical reporters and subsequent ligation to fluorescent probes. This technique has enabled visualization of glycans in living cells and in live organisms such as zebrafish. Molecular imaging with chemical reporters offers a new avenue for probing changes in the glycome that accompany development and disease.
引用
收藏
页码:12 / 17
页数:6
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