Enhancing Enzymatic Bioconjugation Efficiency via Computer-Based Installation of a Substrate Recruitment Domain

Enzyme mediated bioconjugation provides a method for easy and rapid formation of protein-protein and protein-small molecule conjugates under mild conditions. Promiscuous enzymes are of particular interest because they can catalyze conjugation reactions on a broad set of substrates. However, this promiscuity carries the risk of undesirable off-target modifications. To mitigate this effect, we used computational design to install a substrate recruitment domain (SRD) onto the promiscuous enzyme, tyrosinase. The redesigned tyrosinase, called design42 (D42), preferentially modifies tyrosine residues adjacent to a 6-amino acid recognition motif/sequence (RS) that is bound by the SRD. Incorporation of the recognition sequence along with a neighboring tyrosine in peptides or proteins allows for rapid D42-mediated conversion of the tyrosine to an orthoquinone, which can be selectively modified with a variety of nucleophiles. We demonstrate the utility of our design system by rapidly installing cytotoxic molecules on a monoclonal antibody.

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Publication Details

Journal
Bioconjugate Chemistry
Published
2026-03-17
DOI
https://doi.org/10.1021/acs.bioconjchem.5c00468
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
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article

Enhancing Enzymatic Bioconjugation Efficiency via Computer-Based Installation of a Substrate Recruitment Domain

Zhiyuan Yao, Jonathan M. Ellis, Amelia C. McCue, Satish K. Nair et al.
Bioconjugate Chemistry
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Enhancing Enzymatic Bioconjugation Efficiency via Computer-Based Installation of a Substrate Recruitment Domain

Zhiyuan Yao, Jonathan M. Ellis, Amelia C. McCue, Satish K. Nair, Albert A. Bowers, Kaylee P. Kuzelka, Brian Kuhlman, Christopher Shelby, Rodney Park
article en

Abstract

Enzyme mediated bioconjugation provides a method for easy and rapid formation of protein-protein and protein-small molecule conjugates under mild conditions. Promiscuous enzymes are of particular interest because they can catalyze conjugation reactions on a broad set of substrates. However, this promiscuity carries the risk of undesirable off-target modifications. To mitigate this effect, we used computational design to install a substrate recruitment domain (SRD) onto the promiscuous enzyme, tyrosinase. The redesigned tyrosinase, called design42 (D42), preferentially modifies tyrosine residues adjacent to a 6-amino acid recognition motif/sequence (RS) that is bound by the SRD. Incorporation of the recognition sequence along with a neighboring tyrosine in peptides or proteins allows for rapid D42-mediated conversion of the tyrosine to an orthoquinone, which can be selectively modified with a variety of nucleophiles. We demonstrate the utility of our design system by rapidly installing cytotoxic molecules on a monoclonal antibody.

Bioconjugate Chemistry
University of North Carolina at Chapel Hill (US), University of Illinois Urbana-Champaign (US), Quantitative BioSciences (US)
Openalex Percentile: Top 20%
Biochemical and Structural Characterization
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