Réaction #1747873

ord-9445eae1669748aa989cd10668209ced

Équation de réaction

Nc1nc2c(c(=O)[nH]1)N=C(CNc1ccc(C(=O)N[C@@H](CCC(=O)[O-])C(=O)O)cc1)CN2
dihydrofolate
COc1ccc(C[C@H](N)C(=O)O)cc1
O-methyl-L-tyrosine
COc1ccc(C[C@H](N)C(=O)O)cc1
O-methyl-L-tyrosine
N[C@@H](Cc1ccc(O)cc1)C(=O)O
tyrosine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONa C-terminal His6 tag was added in order
  2. 2
    Autreto separate the mutant protein from endogenous E

Mode opératoire

To further demonstrate that the observed phenotype is due to the site-specific incorporation of O-methyl-L-tyrosine by the orthogonal mtRNACUATyr/mutant TyrRS (LWJ16) pair in response to an amber stop codon, an O-methyl-L-tyrosine mutant of dihydrofolate reductase (DHFR) was generated and characterized. The third codon of the E. coli DHFR gene (a permissive site) was mutated to TAG and a C-terminal His6 tag was added in order to separate the mutant protein from endogenous E. coli DHFR. As a control, the mtRNACUATyr was coexpressed with the wild type M. jannaschii TyrRS, resulting in efficient suppression of the nonsense codon in DHFR with tyrosine. See FIG. 2. When the mutant TyrRS (LWJ16) was expressed in the presence of mtRNACUATyr and 1 mM O-methyl-L-tyrosine in liquid GMML growth media, full length DHFR was also produced and could be purified by Ni affinity chromatography with an isolated yield of 2 mg/liter.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08030074B2uspto-grants-2011_10