Here's how site specific incorporations of unnatural amino acids (UAAs) works:
1) You take a plasmid containing your gene of interest and find the codon corresponding to the amino acid that you want to mutate.
2) You change that codon to a TAG sequence on the coding strand (see the my post in the thread on
site-directed mutagenesis for how to do this). This results in TAG on the coding strand of the DNA, CTA on the non-coding strand, and UAG on the corresponding mRNA.
3) You introduce this plasmid into a special strain of
E. coli that has been engineered to allow for UAA incorporation. This strain will have three important characteristics:
A) UAG is normally a stop codon that would terminate protein synthesis, producing a truncated protein. However, there are strains of
E. coli known as
nonsense suppressor strains that do not recognize certain stop codons correctly. We choose the UAG stop codon because, of the three stop codons, it appears least frequently in the
E. coli genome.
B) The strain will also express an enginneered tRNA that contains a CUA sequence on its anticodon loop. This tRNA will bind to the UAG codon on the mRNA to incorporate the UAA into the protein during ribosomal protein synthesis.
C) Finally, the strain will also have an engineered aminoacyl tRNA synthetase that will attach the UAA to the engineered tRNA.