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.

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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

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article

A Genetically Encoded Redox-Active Nicotinamide Amino Acid

Michael Pigula, Peter G. Schultz, Hengyao You, Yahui Ban
1 citations
Biochemistry
CRISPR and Genetic Engineering
0.23
article

A Genetically Encoded Redox-Active Nicotinamide Amino Acid

Michael Pigula, Peter G. Schultz, Hengyao You, Yahui Ban
article en
1 citations

Abstract

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.

BiochemistryVol. 63(24)
Scripps Institution of Oceanography (US), Torrey Pines Institute For Molecular Studies (US), Scripps (United States) (US)
National Institutes of Health
Zero hunger
Openalex Percentile: Top 41%
CRISPR and Genetic Engineering
0.23
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A Genetically Encoded Redox-Active Nicotinamide Amino Acid — Michael Pigula, Peter G. Schultz, et al. · Biochemistry (2024) | TGRS Research Map | TGRS