生物结合
点击化学
排序酶A
化学
组合化学
分拣酶
环加成
叠氮化物
荧光
体内分布
炔烃
纳米技术
生物化学
材料科学
有机化学
体外
物理
量子力学
细菌蛋白
基因
催化作用
作者
Karen Alt,Brett M. Paterson,Erik Westein,Stacey E. Rudd,Stan Poniger,Shweta Jagdale,Katie Ardipradja,Timothy U. Connell,Guy Y. Krippner,Ashish K. N. Nair,Xiaowei Wang,Henri Tochon‐Danguy,Paul S. Donnelly,Karlheinz Peter,Christoph E. Hagemeyer
标识
DOI:10.1002/ange.201411507
摘要
Abstract A unique two‐step modular system for site‐specific antibody modification and conjugation is reported. The first step of this approach uses enzymatic bioconjugation with the transpeptidase Sortase A for incorporation of strained cyclooctyne functional groups. The second step of this modular approach involves the azide–alkyne cycloaddition click reaction. The versatility of the two‐step approach has been exemplified by the selective incorporation of fluorescent dyes and a positron‐emitting copper‐64 radiotracer for fluorescence and positron‐emission tomography imaging of activated platelets, platelet aggregates, and thrombi, respectively. This flexible and versatile approach could be readily adapted to incorporate a large array of tailor‐made functional groups using reliable click chemistry whilst preserving the activity of the antibody or other sensitive biological macromolecules.
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