Genomic medicine redefined
Our protein editing platform works seamlessly within the cell’s translational machinery to overwrite disease-causing mutations.
An elegant and versatile platform
Our technology makes subtle revisions to the natural rules for protein translation, causing erroneous premature termination signals to be overwritten by insertion of a desired amino acid. This enables the production of complete, functional proteins from faulty genes.
Working with the cell
Rather than making permanent and forceful changes to the cell, our tRNA engineering approach corrects disease-causing mutations without altering DNA or mRNA. This precise but light touch keeps the cell’s natural regulatory processes intact and aids in restoring proper protein function.
