Homo-Oligomerisation in Signal Transduction: Dynamics, Homeostasis, Ultrasensitivity, Bistability. (21st August 2020)
- Record Type:
- Journal Article
- Title:
- Homo-Oligomerisation in Signal Transduction: Dynamics, Homeostasis, Ultrasensitivity, Bistability. (21st August 2020)
- Main Title:
- Homo-Oligomerisation in Signal Transduction: Dynamics, Homeostasis, Ultrasensitivity, Bistability
- Authors:
- Koch, Daniel
- Abstract:
- Graphical abstract: Highlights: Homo-oligomerisation may offer an unexpected variety of signal processing functions. These include: dynamic signal encoding via oligomeric complex size. Homeostatic regulation of monomer concentration. Bistability via pseudo-multisite modification and multi-enzyme regulation. The findings partly explain why homo-oligomerisation is so commonly found in evolution. Abstract: Homo-oligomerisation of proteins is a ubiquitous phenomenon whose exact role remains unclear in many cases. To identify novel functions, this paper provides an exploration of general dynamical mathematical models of homo-oligomerisation. Simulation and analysis of these models show that homo-oligomerisation on its own allows for a remarkable variety of complex dynamic and steady state regulatory behaviour such as transient overshoots or homeostatic control of monomer concentration. If post-translational modifications are considered, however, conventional mass action kinetics lead to thermodynamic inconsistencies due to asymmetric combinatorial expansion of reaction routes. Introducing a conservation principle to balance rate equations re-establishes thermodynamic consistency. Using such balanced models it is shown that oligomerisation can lead to bistability by enabling pseudo-multisite modification and kinetic pseudo-cooperativity via multi-enzyme regulation, thereby constituting a novel motif for bistable modification reactions. Due to these potential signal processingGraphical abstract: Highlights: Homo-oligomerisation may offer an unexpected variety of signal processing functions. These include: dynamic signal encoding via oligomeric complex size. Homeostatic regulation of monomer concentration. Bistability via pseudo-multisite modification and multi-enzyme regulation. The findings partly explain why homo-oligomerisation is so commonly found in evolution. Abstract: Homo-oligomerisation of proteins is a ubiquitous phenomenon whose exact role remains unclear in many cases. To identify novel functions, this paper provides an exploration of general dynamical mathematical models of homo-oligomerisation. Simulation and analysis of these models show that homo-oligomerisation on its own allows for a remarkable variety of complex dynamic and steady state regulatory behaviour such as transient overshoots or homeostatic control of monomer concentration. If post-translational modifications are considered, however, conventional mass action kinetics lead to thermodynamic inconsistencies due to asymmetric combinatorial expansion of reaction routes. Introducing a conservation principle to balance rate equations re-establishes thermodynamic consistency. Using such balanced models it is shown that oligomerisation can lead to bistability by enabling pseudo-multisite modification and kinetic pseudo-cooperativity via multi-enzyme regulation, thereby constituting a novel motif for bistable modification reactions. Due to these potential signal processing capabilities, homo-oligomerisation could play far more versatile roles in signal transduction than previously appreciated. … (more)
- Is Part Of:
- Journal of theoretical biology. Volume 499(2020)
- Journal:
- Journal of theoretical biology
- Issue:
- Volume 499(2020)
- Issue Display:
- Volume 499, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 499
- Issue:
- 2020
- Issue Sort Value:
- 2020-0499-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-08-21
- Subjects:
- Protein complexes -- Mathematical modelling -- Dynamic signal encoding -- Post-translational modifications -- Multi-enzyme systems
Biology -- Periodicals
Biological Science Disciplines -- Periodicals
Biology -- Periodicals
Biologie -- Périodiques
Theoretische biologie
Biology
Periodicals
571.05 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00225193/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jtbi.2020.110305 ↗
- Languages:
- English
- ISSNs:
- 0022-5193
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5069.075000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13433.xml