MOTIVATION: Studying biological systems, not just at an individual component level but at a system-wide level, gives us great potential to understand fundamental functions and essential biological properties. Despite considerable advances in the topological analysis of metabolic networks, inadequate knowledge of the enzyme kinetic rate laws and their associated parameter values still hampers large-scale kinetic modelling. Furthermore, the integration of gene expression and protein levels into kinetic models is not straightforward. RESULTS: The focus of our research is on streamlining the construction of large-scale kinetic models. A novel software tool was developed, which enables the generation of generic rate equations for all reactions in a model. It encompasses an algorithm for estimating the concentration of proteins for a reaction to reach a particular steady state when kinetic parameters are unknown, and two robust methods for parameter estimation. It also allows for the seamless integration of gene expression or protein levels into a reaction and can generate equations for both transcription and translation. We applied this methodology to model the yeast glycolysis pathway; our results show that the behaviour of the system can be accurately described using generic kinetic equations. AVAILABILITY AND IMPLEMENTATION: The software tool, together with its source code in Java, is available from our project web site at http://www.bioinf.manchester.ac.uk/schwartz/grape CONTACT: jean-marc.schwartz@manchester.ac.uk SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
MOTIVATION: Studying biological systems, not just at an individual component level but at a system-wide level, gives us great potential to understand fundamental functions and essential biological properties. Despite considerable advances in the topological analysis of metabolic networks, inadequate knowledge of the enzyme kinetic rate laws and their associated parameter values still hampers large-scale kinetic modelling. Furthermore, the integration of gene expression and protein levels into kinetic models is not straightforward. RESULTS: The focus of our research is on streamlining the construction of large-scale kinetic models. A novel software tool was developed, which enables the generation of generic rate equations for all reactions in a model. It encompasses an algorithm for estimating the concentration of proteins for a reaction to reach a particular steady state when kinetic parameters are unknown, and two robust methods for parameter estimation. It also allows for the seamless integration of gene expression or protein levels into a reaction and can generate equations for both transcription and translation. We applied this methodology to model the yeast glycolysis pathway; our results show that the behaviour of the system can be accurately described using generic kinetic equations. AVAILABILITY AND IMPLEMENTATION: The software tool, together with its source code in Java, is available from our project web site at http://www.bioinf.manchester.ac.uk/schwartz/grape CONTACT: jean-marc.schwartz@manchester.ac.uk SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Authors: Peter Li; Joseph O Dada; Daniel Jameson; Irena Spasic; Neil Swainston; Kathleen Carroll; Warwick Dunn; Farid Khan; Naglis Malys; Hanan L Messiha; Evangelos Simeonidis; Dieter Weichart; Catherine Winder; Jill Wishart; David S Broomhead; Carole A Goble; Simon J Gaskell; Douglas B Kell; Hans V Westerhoff; Pedro Mendes; Norman W Paton Journal: BMC Bioinformatics Date: 2010-11-29 Impact factor: 3.169