Translational control of enzyme scavenger expression with toxin-induced micro RNA switches

Abstract Biological computation requires in vivo control of molecular behavior to progress development of autonomous devices. miRNA switches represent excellent, easily engineerable synthetic biology tools to achieve user-defined gene regulation. Here we present the construction of a synthetic netwo...

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Main Authors: Nina M. Pollak, Justin J. Cooper-White, Joanne Macdonald
Format: Article
Language:English
Published: Nature Publishing Group 2021-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-81679-6
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spelling doaj-b0e97f0d97544fadb1b5f8b8a0c9ba752021-01-31T16:24:48ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111210.1038/s41598-021-81679-6Translational control of enzyme scavenger expression with toxin-induced micro RNA switchesNina M. Pollak0Justin J. Cooper-White1Joanne Macdonald2Genecology Research Centre, University of the Sunshine CoastAustralian Institute for Bioengineering and Nanotechnology, The University of QueenslandGenecology Research Centre, University of the Sunshine CoastAbstract Biological computation requires in vivo control of molecular behavior to progress development of autonomous devices. miRNA switches represent excellent, easily engineerable synthetic biology tools to achieve user-defined gene regulation. Here we present the construction of a synthetic network to implement detoxification functionality. We employed a modular design strategy by engineering toxin-induced control of an enzyme scavenger. Our miRNA switch results show moderate synthetic expression control over a biologically active detoxification enzyme molecule, using an established design protocol. However, following a new design approach, we demonstrated an evolutionarily designed miRNA switch to more effectively activate enzyme activity than synthetically designed versions, allowing markedly improved extrinsic user-defined control with a toxin as inducer. Our straightforward new design approach is simple to implement and uses easily accessible web-based databases and prediction tools. The ability to exert control of toxicity demonstrates potential for modular detoxification systems that provide a pathway to new therapeutic and biocomputing applications.https://doi.org/10.1038/s41598-021-81679-6
collection DOAJ
language English
format Article
sources DOAJ
author Nina M. Pollak
Justin J. Cooper-White
Joanne Macdonald
spellingShingle Nina M. Pollak
Justin J. Cooper-White
Joanne Macdonald
Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
Scientific Reports
author_facet Nina M. Pollak
Justin J. Cooper-White
Joanne Macdonald
author_sort Nina M. Pollak
title Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
title_short Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
title_full Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
title_fullStr Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
title_full_unstemmed Translational control of enzyme scavenger expression with toxin-induced micro RNA switches
title_sort translational control of enzyme scavenger expression with toxin-induced micro rna switches
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-01-01
description Abstract Biological computation requires in vivo control of molecular behavior to progress development of autonomous devices. miRNA switches represent excellent, easily engineerable synthetic biology tools to achieve user-defined gene regulation. Here we present the construction of a synthetic network to implement detoxification functionality. We employed a modular design strategy by engineering toxin-induced control of an enzyme scavenger. Our miRNA switch results show moderate synthetic expression control over a biologically active detoxification enzyme molecule, using an established design protocol. However, following a new design approach, we demonstrated an evolutionarily designed miRNA switch to more effectively activate enzyme activity than synthetically designed versions, allowing markedly improved extrinsic user-defined control with a toxin as inducer. Our straightforward new design approach is simple to implement and uses easily accessible web-based databases and prediction tools. The ability to exert control of toxicity demonstrates potential for modular detoxification systems that provide a pathway to new therapeutic and biocomputing applications.
url https://doi.org/10.1038/s41598-021-81679-6
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