Light-Induced Nanobody-Mediated Targeted Protein Degradation for Metabolic Flux Control

In metabolic engineering, increasing chemical production usually involves manipulating the expression levels of key enzymes. However, limited synthetic tools exist for modulating enzyme activity beyond the transcription level. Inspired by natural post-translational mechanisms, we present targeted enzyme degradation mediated by optically controlled nanobodies. We applied this method to a branched biosynthetic pathway, deoxyviolacein, and observed enhanced product specificity and yield. We then extend the biosynthesis pathway to violacein and show how simultaneous degradation of two target enzymes can further shift production profiles. Through the redirection of metabolic flux, we demonstrate how targeted enzyme degradation can be used to minimize unwanted intermediates and boost the formation of desired products.

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Publication Details

Journal
ACS Synthetic Biology
Published
2024-11-11
DOI
https://doi.org/10.1021/acssynbio.4c00552
Citations
8
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
1.87

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article

Light-Induced Nanobody-Mediated Targeted Protein Degradation for Metabolic Flux Control

Stéphanie Jung, Allison Y. Tang, José L. Avalos‬, César Carrasco‐López
8 citations
ACS Synthetic Biology
Photosynthetic Processes and Mechanisms
1.87
article

Light-Induced Nanobody-Mediated Targeted Protein Degradation for Metabolic Flux Control

Stéphanie Jung, Allison Y. Tang, José L. Avalos‬, César Carrasco‐López
article en
8 citations

Abstract

In metabolic engineering, increasing chemical production usually involves manipulating the expression levels of key enzymes. However, limited synthetic tools exist for modulating enzyme activity beyond the transcription level. Inspired by natural post-translational mechanisms, we present targeted enzyme degradation mediated by optically controlled nanobodies. We applied this method to a branched biosynthetic pathway, deoxyviolacein, and observed enhanced product specificity and yield. We then extend the biosynthesis pathway to violacein and show how simultaneous degradation of two target enzymes can further shift production profiles. Through the redirection of metabolic flux, we demonstrate how targeted enzyme degradation can be used to minimize unwanted intermediates and boost the formation of desired products.

ACS Synthetic BiologyVol. 13(12)
Princeton University (US)
Princeton University
Zero hunger
Openalex Percentile: Top 14%
Photosynthetic Processes and Mechanisms
1.87
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