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An enzyme-based biosensor for monitoring and engineering protein stability in vivo
by
Mencius, Jun
, Ren, Chang
, Wen, Xin
, Quan, Shu
in
Acid Anhydride Hydrolases - chemistry
/ Acid Anhydride Hydrolases - genetics
/ Acylphosphatase
/ Biochemistry
/ Biological Sciences
/ Biosensing Techniques
/ Catalytic Domain
/ Directed Molecular Evolution - methods
/ Escherichia coli
/ Fluorescence
/ High-Throughput Screening Assays
/ Humans
/ Methyltransferases - chemistry
/ Methyltransferases - genetics
/ Mutation
/ Protein Engineering
/ Protein Stability
2021
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An enzyme-based biosensor for monitoring and engineering protein stability in vivo
by
Mencius, Jun
, Ren, Chang
, Wen, Xin
, Quan, Shu
in
Acid Anhydride Hydrolases - chemistry
/ Acid Anhydride Hydrolases - genetics
/ Acylphosphatase
/ Biochemistry
/ Biological Sciences
/ Biosensing Techniques
/ Catalytic Domain
/ Directed Molecular Evolution - methods
/ Escherichia coli
/ Fluorescence
/ High-Throughput Screening Assays
/ Humans
/ Methyltransferases - chemistry
/ Methyltransferases - genetics
/ Mutation
/ Protein Engineering
/ Protein Stability
2021
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An enzyme-based biosensor for monitoring and engineering protein stability in vivo
by
Mencius, Jun
, Ren, Chang
, Wen, Xin
, Quan, Shu
in
Acid Anhydride Hydrolases - chemistry
/ Acid Anhydride Hydrolases - genetics
/ Acylphosphatase
/ Biochemistry
/ Biological Sciences
/ Biosensing Techniques
/ Catalytic Domain
/ Directed Molecular Evolution - methods
/ Escherichia coli
/ Fluorescence
/ High-Throughput Screening Assays
/ Humans
/ Methyltransferases - chemistry
/ Methyltransferases - genetics
/ Mutation
/ Protein Engineering
/ Protein Stability
2021
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An enzyme-based biosensor for monitoring and engineering protein stability in vivo
Journal Article
An enzyme-based biosensor for monitoring and engineering protein stability in vivo
2021
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Overview
Protein stability affects the physiological functions of proteins and is also a desirable trait in many protein engineering tasks, yet improving protein stability is challenging because of limitations in methods for directly monitoring protein stability in cells. Here, we report an in vivo stability biosensor wherein a protein of interest (POI) is inserted into a microbial enzyme (CysGA) that catalyzes the formation of endogenous fluorescent compounds, thereby coupling POI stability to simple fluorescence readouts. We demonstrate the utility of the biosensor in directed evolution to obtain stabilized, less aggregation-prone variants of two POIs (including nonamyloidogenic variants of human islet amyloid polypeptide). Beyond engineering applications, we exploited our biosensor in deep mutational scanning for experimental delineation of the stability-related contributions of all residues throughout the catalytic domain of a histone H3K4 methyltransferase, thereby revealing its scientifically informative stability landscape. Thus, our highly accessible method for in vivo monitoring of the stability of diverse proteins will facilitate both basic research and applied protein engineering efforts.
Publisher
National Academy of Sciences
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