半胱氨酸
荧光团
化学
氟苯
取代基
蛋白酵素
生物素
叠氮化物
组合化学
荧光
生物化学
立体化学
酶
有机化学
物理
苯
量子力学
作者
Ahmed M. Embaby,Sanne Schoffelen,Christian Kofoed,Morten Meldal,Frederik Diness
标识
DOI:10.1002/anie.201712589
摘要
Abstract Fluorobenzene probes for protein profiling through selective cysteine labeling have been developed by rational reactivity tuning. Tuning was achieved by selecting an electron‐withdrawing para substituent in combination with variation of the number of fluorine substituents. Optimized probes chemoselectively arylated cysteine residues in proteins under aqueous conditions. Probes linked to azide, biotin, or a fluorophore were applicable to labeling of eGFP and albumin. Selective inhibition of cysteine proteases was also demonstrated with the probes. Additionally, probes were tuned for site‐selective labeling of cysteine residues and for activity‐based protein profiling in cell lysates.
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