Site-Specific Incorporation of Fluorotyrosines into Proteins in Escherichia coli by Photochemical Disguise

被引:35
|
作者
Wilkins, Bryan J. [2 ]
Marionni, Samuel [2 ]
Young, Douglas D. [1 ]
Liu, Jia [2 ]
Wang, Yan [2 ]
Di Salvo, Martino L. [3 ,4 ]
Deiters, Alexander [1 ]
Cropp, T. Ashton [2 ]
机构
[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] Univ Roma La Sapienza, Dipartimento Sci Biochim, I-00185 Rome, Italy
[4] Univ Roma La Sapienza, Inst Pasteur, Fdn Cenei Bolognetti, I-00185 Rome, Italy
基金
美国国家科学基金会;
关键词
GREEN FLUORESCENT PROTEIN; GENETIC-CODE; AMINO-ACIDS; TYROSINE;
D O I
10.1021/bi100013s
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
Fluorinated analogues of tyrosine call be used to Manipulate the electronic environments of protein active sites. The ability to selectively Mutate tyrosine residues to fluorotyrosines is limited, however, and call Currently only be achieved through the total synthesis of proteins. As it general Solution to this problem, we genetically encoded the unnatural amino acids o-nitrobenzyl-2-fluorotyrosine, -3-fluorotyrosine, and -2,6-difluorotyrosine in Escherichia coli. These amino acids are disguised from recognition by the endogenous protein biosynthetic machinery, effectively preventing global incorporation of fluorotyrosine into proteins.
引用
收藏
页码:1557 / 1559
页数:3
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