Building better bioorthogonal reactions

被引:80
作者
Shih, Hui-Wen [1 ]
Kamber, David N. [1 ]
Prescher, Jennifer A. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
关键词
IN-VIVO; PHOTOCLICK-CHEMISTRY; CHEMICAL REPORTERS; TRANS-CYCLOOCTENE; CLICK CHEMISTRY; DIAZO-COMPOUNDS; LIGATION; DESIGN; AZIDE; STRAIN;
D O I
10.1016/j.cbpa.2014.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the past two decades, there has been intense interest in designing and implementing selective (bioorthogonal) reactions for biomolecule tracking. Here we review the most widely used bioorthogonal chemistries in live cells and animals, drawing particular attention to the unique functional groups underlying these transformations. We also describe recent efforts to tune functional group reactivities and stabilities to access even more rapid and selective chemistries. Last, we highlight ongoing challenges in identifying new bioorthogonal reagents and combinations of reactions that can be used concurrently to tag multiple biomolecules.
引用
收藏
页码:103 / 111
页数:9
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