A Genetically Encoded Redox-Active Nicotinamide Amino Acid
Nicotinamide-containing cofactors play an essential role in many enzymes that catalyze two-electron redox reactions. However, it is difficult to engineer nicotinamide binding sites into proteins due to the extended nature of the cofactor-protein interface and the precise orientation of the nicotinamide moiety required for efficient electron transfer to or from the substrate. To address these challenges, we genetically encoded a noncanonical amino acid (ncAA) bearing a nicotinamide side chain in bacteria. This redox-active amino acid, termed Nic1, exhibits similar electrochemical properties to the natural cofactor nicotinamide adenine dinucleotide (NAD<sup>+</sup>). Nic1 can be reversibly reduced and oxidized using chemical reagents both free in solution and when incorporated into a model protein. This genetically encodable cofactor can be introduced into proteins in a site-specific fashion and may serve as a tool to study electron-transfer mechanisms in enzymes and to engineer redox-active proteins.
Authors
- Michael Pigula (ORCID: https://orcid.org/0000-0001-6121-9995)
- Peter G. Schultz (ORCID: https://orcid.org/0000-0003-3188-1202)
- Hengyao You
- Yahui Ban (ORCID: https://orcid.org/0009-0006-2122-3395)
Institutions
- Scripps Institution of Oceanography (US)
- Torrey Pines Institute For Molecular Studies (US)
- Scripps (United States) (US)
Publication Details
- Journal
- Biochemistry
- Published
- 2024-11-25
- DOI
- https://doi.org/10.1021/acs.biochem.4c00530
- Citations
- 1
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.23
Funders
- National Institutes of Health