- Analyzing (BBa_K2201201, BBa_K2201202): Two different ncAAs are incorporated which are labeled with fluorophores in a chemically reaction. With the help of Foerster Resonance Energy Transfer (FRET), the distance between the amino acids could be measured, to get information about the conformation.
- Photoswitching (BBa_K2201207): A photoisomerisable amino acid could be incorporated which changes its conformation when it is irradiated with light of different wavelengths. This conformation change can be used to inhibit the functionality of the target protein, so that reactions can be switched on and off on the protein level using only light exposure.
- Labeling (BBa_K2201204): A fluorescent amino acid could be used to label the target protein in vivo. The advantages compared to fluorescent proteins lay in the smaller size of the fluorescent amino acid.
- Photolysis (BBa_K2201200): Photolysis amino acids break the peptide backbone at the position they were incorporated. This cleaving could be used to activate or deactivate proteins.
- Fusing (BBa_K2201208, BBa_K2201302): Two ncAAs which form a specific covalent bond between each other can be used to fuse proteins together or immobilize the target protein, independent of the C- or N-termini.
Team:Bielefeld-CeBiTec/Project/toolbox
Toolbox Overview
Toolbox
Our toolbox for advanced protein design consists of eight different tRNA/aminacyl-synthetases (aaRS), each capable of loading a specific non-canonical amino acid (ncAA) to the amber tRNA or the less used leucine tRNA to incorporate these ncAAs into all types of target proteins. The aaRSs are provided as parts in the Registry of Standard Biological Parts, so that further iGEM teams will have the benefit of using our toolbox to improve their projects. The properties we integrated in our toolbox are Analyzing, Photoswitching, Labeling, Photolysis and Fusing (Figure 1).
Figure 1: Overview of the different functions provided by specific ncAAs. We want to integrate plasmids with the sequences of specific synthetases into our toolbox and provide them for the iGEM as well as the synthetic biology community.
We hope that our toolbox will be used frequently by future iGEM-teams and help them at their projects. We also wish that they will add new synthetases for other ncAAs and thus expand the possibilities of further applications in protein design.
Two Different Ways on how to Incorporate ncAAs
Generally the incorporation in response to the amber stop codon (TAG) and the less used leucine codon (CTA) limits the number of different non-canonical amino acids to two. The incorporation through these codons also inhibits the growth of culture, like described in the translation mechanism. An additional base in the DNA would circumvent these problems and offers 64 new different codons to incorporate different ncAAs like shown in Figure 2. Both, the incorporation through codons containing an unnatural base and the incorporation through a less used existing codon are ways to incorporate ncAAs.
Figure 2: Expanded code sun. Representation of the code sun after the incorporation of one new unnatural base to expand the genetic code and create new blank codons (purple) that can be used to evolve aaRS to enable ncAAs for advanced protein design.
