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.
Site-Specific Incorporation of Fluorotyrosines into Proteins in Escherichia coli by Photochemical Disguise / Bryan J., Wilkins; Samuel, Marionni; Douglas D., Young; Jia, Liu; Yan, Wang; DI SALVO, Martino Luigi; Alexander, Deiters; T., Ashton Cropp. - In: BIOCHEMISTRY. - ISSN 0006-2960. - 49:8(2010), pp. 1557-1559. [10.1021/bi100013s]
Site-Specific Incorporation of Fluorotyrosines into Proteins in Escherichia coli by Photochemical Disguise
DI SALVO, Martino Luigi;
2010
Abstract
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.