Abstract
Genome-scale metabolic networks let us understand the behaviour of the metabolism in the cells of living organisms. The availability of great amounts of such data gives the scientific community the opportunity to infer in silico new metabolic knowledge. Elementary Flux Modes (EFM) are minimal contained pathways or subsets of a metabolic network that are very useful to achieving the comprehension of a very specific metabolic function (as well as dysfunctions), and to get the knowledge to develop new drugs. Metabolic networks can have large connectivity and, therefore, EFMs resolution faces a combinational explosion challenge to be solved. In this paper we propose a new approach to obtain EFMs based on graph theory, the balanced graph concept and the shortest path between end nodes. Our proposal uses the shortest path between end nodes (input and output nodes) that finds all the pathways in the metabolic network and is able to prioritise the pathway search accounting the biological mean pursued. Our technique has two phases, the exploration phase and the characterisation one, and we show how it works in a well-known case study. We also demonstrate the relevance of the concept of balanced graph to achieve to the full list of EFMs.
Highlights
Cellular metabolism is the set of biochemical enzyme-catalysed reactions involved in the generation of nutrients and energy necessary for the cells in living organisms
Despite the development of novel methods using state of the art computational techniques expediting their application in larger networks [11], this family of algorithms fails on genome-scale metabolic network (GSMN) using standard computers, because of the combinatorial explosion in the number of Elementary Flux Modes (EFM) [4]
Constraint-based modelling (CBM) starts with a stoichiometric matrix S whose values are the stoichiometric coefficients for metabolites on each reaction
Summary
Cellular metabolism is the set of biochemical enzyme-catalysed reactions involved in the generation of nutrients and energy necessary for the cells in living organisms. Despite the development of novel methods using state of the art computational techniques expediting their application in larger networks [11], this family of algorithms fails on GSMNs using standard computers, because of the combinatorial explosion in the number of EFMs [4]. In this light, several methods have been recently proposed to determine a subset of EFMs in GSMNs [12,13,14,15]. The connectedness and minimality of solutions have to be treated complementarily during the process
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