Kinetic Switches: Exploiting Feedback in Enzyme Microparticles

Lead Research Organisation: University of Sheffield
Department Name: Chemical & Biological Engineering

Abstract

Many biological processes require a rapid transition from one chemical state to another following a supercritical stimulus. These kinetically-controlled cell switches are driven by feedback such as autocatalysis, when a reaction is catalysed by its product. Feedback also lies at the heart of synchronisation of activity in cellular systems such as bacteria and yeast. There has been great interest in the design of reaction networks that produce feedback-driven behaviour, for example, genetic circuits were developed to create a toggle switch, chemical oscillations and synchronisation of oscillations in E. coli cells.

Through computational studies and experiments, we will design bio-inspired switches combining two components: feedback in the reaction kinetics and compartmentalisation of the reaction in microparticles. This research will provide insight into biological self-organisation as well as having potential applications in analytical or "smart" materials science.

The first component of the research involves designing novel reaction networks for chemical feedback and for this we will use nature's catalysts: enzymes. Enzymes offer specificity, efficiency and biocompatibility for widespread applications such as sensors, drug delivery devices and bio-reactors but the wealth of behaviour associated with autocatalysis has yet to be exploited. We will investigate possible advantages such as such as a fast, robust response to a chemical signal in the presence of noise.

In order to create a cellular switch, the enzyme catalyst for the reaction will be immobilised in microparticles. When immersed in a bath of reactants, the microparticles obtain chemical "fuel" from the surrounding solution, naturally maintaining the system far-from-equilibrium in a similar manner to cells. By manipulation of the kinetics, exciting features such as a chemical switch, hysteresis, chemical pulses, patterns or self-motion of the microparticles are possible. Groups of enzyme microparticles interact with each other via the release of chemicals into the surrounding solution, thus creating a new opportunity for the examination of collective behaviours and self-organisation in bio-inspired cellular systems.

Planned Impact

The science of far-from-equilibrium self-organisation, or "complexity science", is of great interest to the general scientific community, as similar behaviours arising from feedback are observed in physics, chemistry, biology as well as the social sciences and are described by underlying mathematical principles. Recently, a new European initiative Euro-Chemistry held a meeting that "highlighted Complexity in Chemistry as one of the important areas where chemistry, in a collaborative effort with mathematics, must focus". This meeting also recognised that nonlinear chemical reactions, i.e. systems with feedback, are fundamental to this effort. We will produce a suite of enzyme reaction networks showing feedback-driven behaviour in silico, and bio-inspired enzyme microparticles that exhibit complex behaviour. Although our research is intended to uncover fundamental principles in far-from-equilibrium nonlinear systems, enzyme autocatalytic reactions and microparticles have potential applications in analytical and "smart" materials science. The research will therefore impact on a wide audience.

The development of autocatalytic enzyme microparticles will impact on scientists driven by a desire to mimic the complex structure and function observed in biology for useful applications. Although enzyme microparticles have been designed for a number of biotechnological applications, such as sensors, drug delivery devices and bio-reactors, the wealth of behaviour associated with autocatalytic reactions has yet to be exploited. Enzymes offer specificity, efficiency and biocompatibility for these applications; feedback gives potential advantages such as fast robust response over a wide range of conditions and in the presence of noise; periodic release of a chemical or synchronised activity overcoming diversity in a group of particles and self-motion of a particle. All of these features are well investigated in biological cell models but would be novel in applications utilising microparticles.

The researchers employed on the project will work as a cross-department, interdisciplinary team and will be trained in the tools of complexity/systems science. They will benefit from the combination of computational (kinetic) modelling and microparticle experiments with resulting skills that could be applied in many employment sectors. Additionally, project-related activities will be offered to PhD students, masters' and summer project students as well as to undergraduates through coursework.

The project is expected to produce visual results that can be communicated to the general public as well as resources that can be used to inspire young people into science. We will engage with local artists to bring particle behaviour to a wider audience through art instillations combining sound with oscillating particles. We will also offer a project-related workshop at science fairs and University initiatives. This will involve development of very a simple microfluidics device for coloured, responsive alginate microparticles, intended to highlight use of edible particles for healthcare, food science and sensing.

Publications

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Ashkenasy G (2017) Systems chemistry. in Chemical Society reviews

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Bohner B (2020) Periodic Nucleation of Calcium Phosphate in a Stirred Biocatalytic Reaction. in Angewandte Chemie (International ed. in English)

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Bubanja I (2017) Kinetics of the urea-urease clock reaction with urease immobilized in hydrogel beads in Reaction Kinetics, Mechanisms and Catalysis

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Bánsági T (2017) Switches induced by quorum sensing in a model of enzyme-loaded microparticles. in Journal of the Royal Society, Interface

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Bánsági T (2018) Exploitation of Feedback in Enzyme-catalysed Reactions in Israel Journal of Chemistry

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Bánsági T (2014) Role of differential transport in an oscillatory enzyme reaction. in The journal of physical chemistry. B

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Jee E (2016) Temporal Control of Gelation and Polymerization Fronts Driven by an Autocatalytic Enzyme Reaction. in Angewandte Chemie (International ed. in English)

 
Description Chemical systems that remain kinetically dormant until activated have numerous applications in materials science. Herein we present a method for the control of gelation that exploits an inbuilt switch: the increase in pH after an induction period in the urease-catalyzed hydrolysis of urea was used to trigger the base-catalyzed Michael addition of a water-soluble trithiol to a polyethylene glycol diacrylate. The time to gelation (minutes to hours) was either preset through the initial concentrations or the reaction was initiated locally by a base, thus resulting in polymerization fronts that converted the mixture from a liquid into a gel (ca. 0.1mm min-1). The rate of hydrolytic degradation of the hydrogel depended on the initial concentrations, thus resulting in a gel lifetime of hours to months. In this way, temporal programming of gelation was possible under mild conditions by using the output of an autocatalytic enzyme reaction to drive both the polymerization and subsequent degradation of a hydrogel.
Exploitation Route Many materials chemistry applications require initial slow reaction followed by rapid curing such as adhesives, coatings, sealants and injectable bio-medical formulations; in the latter subsequent degradation of the gel for drug release is also desirable. We have shown how amplification of a chemical signal might be translated into a physical response: an autocatalytic enzyme reaction was used to drive time-lapse gelation and frontal polymerization. The gel lifetime was also controlled through the initial concentrations of the enzyme reaction and the thiol. Coupling autocatalytic reactions with physical processes has generated pulses of precipitates,bio-inspired chemomechanical devices, thiol-acrylate microparticles and periodic nanoparticle aggregation, however these systems involved harsh chemicals that limit their use in applications. We used an enzyme-catalyzed reaction with a water-soluble thiol and acrylate to create a gelation process that operates under ambient, aqueous phase conditions.
Our system does not require radical initiators or high temperature but operates using an inbuilt pH switch. Other autocatalytic enzyme reactions, such as the glucose-oxidase reaction, involve base to acid switches that might be used in conjunction with acid-catalyzed polymerization. This systems chemistry approach to transient gelation has numerous attractive features for bio-inspired, bio-compatible materials applications.
Sectors Healthcare,Manufacturing, including Industrial Biotechology

 
Description H2020-MSCA-IF-2017
Amount € 183,454 (EUR)
Organisation European Commission 
Department Horizon 2020
Sector Public
Country European Union (EU)
Start 12/2018 
End 12/2020
 
Description H2020-MSCA-ITN-2018
Amount € 4,076,237 (EUR)
Funding ID 812868 
Organisation University of Sheffield 
Sector Academic/University
Country United Kingdom
Start 04/2019 
End 11/2022
 
Description polymers 
Organisation Louisiana State University
Department Department of Chemistry
Country United States 
Sector Academic/University 
PI Contribution Modelling
Collaborator Contribution Experiments
Impact Hu, G.; Bounds, C.; Pojman, J. A.; Taylor, A. F. Time-Lapse Thiol-Acrylate Polymerization Using a pH Clock Reaction J. Polym. Sci. Pol. Chem. 2010, 48, 2955. Hu, G.; Pojman, J.; Wrobel, M. M.; Scott, S. K.; Taylor, A. F. Base-Catalyzed Feedback in the Urea-Urease Reaction J. Phys. Chem. B 2010, 114, 14059. Wrobel MM, Bánsági Jr T, Scott SK, Taylor AF, Bounds CO, Carranzo A, Pojman JA. pH wave-front propagation in the urea-urease reaction. Biophysical Journal 103(3):610-615
Start Year 2010