Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Genetic Code Compression and Expansion

In plain English

AI plain-English summary

A synthetic E. coli genome now uses 61 codons instead of the standard 64, freeing up three blank codons for a new kind of protein engineering. This matters because standard genetic code expansion is limited to inserting one artificial building block—a non-canonical amino acid—into a protein at a time, because only the amber stop codon is typically available as a blank slot. The compressed genome, called Syn61, creates multiple blank codons that can each be reassigned to a different non-canonical amino acid, allowing researchers to build proteins with several unnatural components simultaneously. If successful, this work could dramatically expand the range of proteins that can be engineered with novel chemical properties. The immediate impact is on fundamental science—enabling experiments that were previously impossible. In the longer term, the ability to encode multiple artificial amino acids into a single protein could lead to new classes of enzymes, materials, or therapeutic proteins with functions that natural proteins cannot perform. The project also aims to discover additional codon compression schemes, potentially creating even more blank codons for future reassignment.

View original technical description
Genetic code expansion enables the site-specific, incorporation of non-canonical amino acids (ncAAs) into proteins, and has enabled diverse biological discoveries. Most experiments incorporate ncAAs in response to amber stop codons. This strategy is limited to incorporating one type of ncAAs into a protein at a time, and there are no other natural blank codons that can be used for ncAA incorporation. We synthesized a 4 Mb E. coli genome with a compressed genetic code, through the genome-wide substitution of three target codons by defined synonyms. The resulting cell, Syn61, uses 61 codons to encode the 20 canonical amino acids. In Aim 1 we address the limitations of genetic code expansion by encoding multiple distinct ncAAs in response to blank codons in Syn61. This dramatically expands the applications of ncAA incorporation. The recoding of Syn61 was based on the prior identification of a synonymous codon compression scheme (a rule that defines which codons to remove and which codons to replace them with). In Aim 2 and Aim 3 we systematically discover allowed synonymous codon compression schemes that we use to create deeply compressed synthetic genomes using accelerated genome synthesis methods. This creates more blank codons that may be reassigned to ncAAs.

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Researchers

Jason Chin (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Genetic Code Expansion in Catalysis
Expanding the Genetic Code of a Synthetic Yeast
Directed Evolution of an Orthogonal Quadruplet Codon-based Genetic Code
Rewriting the genetic code through aminoacyl tRNA synthetase engineering
Double Incorporation of Non-Canonical Amino Acids in an Animal and its Application for Precise and Independent Optical Control of Two Target Genes

Original classification

Investigator Award in Science

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