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Metabolomic systems biology analysis of differentiation in trypanosomes

Reference	BB/F005679/1
Principal Investigator / Supervisor	Professor Mike Barrett
Co-Investigators / Co-Supervisors	Professor David Gilbert
Institution	University of Glasgow
Department	Institute of Biomedical & Life Sciences
Funding type	Research
Value (£)	457,047
Status	Completed
Type	Research Grant
Start date	17/03/2008
End date	16/01/2012
Duration	46 months

Abstract

A limitation in modelling of biochemical networks relates to a lack of general compatibility between static and dynamic modelling. We aim to reduce this gap and provide the means by which biochemists move seamlessly from the global view of metabolism provided by static modelling, to a detailed representation derived from dynamic modelling. We will design and evaluate new combinatory and visual means to detect, within large networks, modules corresponding to key pathways involved in the system under study. We will then model a selected pathway using dynamic modelling and then check it experimentally. We will focus on the protozoan, Trypanosoma brucei, an extraordinary model system which undergoes a complex life cycle alternating between the divergent environments of the mammalian bloodstream and the tsetse fly. As a consequence, trypanosomes remodel their metabolism to adapt to these incongruent conditions. Once within those environments, however, they enjoy relative stability, thus their capacity to retain homeostasis is pre-programmed and their metabolic network is less plastic than those seen in free living organisms like yeast. We will make comprehensive measurements of the trypanosome's metabolome as the parasites transform. Ab initio networks, where individual metabolites are linked by chemical transformations between them, will be constructed along with other networks of metabolites whose abundance changes in a coordinated fashion. Modules, comprising connected metabolites whose abundance changes in a coordinated fashion throughout the differentiation process will be identified and the components of a selected module will be subject to dynamic modelling. Predictions based on the modelling will then guide reverse genetics based experiments to remove genes encoding enzymes central to the modules predicted to be critical to differentiation, and assessing their impact on differentation and the metabolome..

Summary

Systems biology is a term that has been coined to describe work that aims to understand biological function through the reconstruction of the component elements that comprise a given system. At the level of the cell, a basic unit from which all living organisms are made, this approach has become feasible since it has become commonplace to identify all of the genes in a given cell type, follow how those genes are turned on and to measure the proteins encoded by the genes. It is also possible to measure the small chemicals that maintain the cell in its viable state. This latter type of measurement has proven more difficult than identification of genes and proteins, because of the chemical complexity of these so-called metabolites. However, technological advances have now enabled comprehensive sampling of these small chemicals, which are, in many regards the actual essence of life (the genes representing a blue print that produces the proteins that build the cellular hardware / while the metabolites that flow within the system represent cellular vitality). We have pioneered technological advances that enable the measurement of thousands of metabolites simultaneously within a given cell. Here we plan to use this technology to identify how metabolites change in a single celled organism, the African trypanosome, as it alternates between the environment of the mammalian bloodstream and that of the tsetse fly vector that carries these parasites between patients. Central to the systems biology approach will be the development of computer software that will enable the reconstruction of large networks of metabolites that are connected to one another and other networks that show how related metabolites change in concentration as the trypanosome moves between the different environments. In addition to these huge networks, we will also develop methods that enable us to identify those parts of the network that change during the differentiation process. We will then focus on selected parts of the network to establish how particular metabolites, that influence the cellular differentiation process, flow through this system and impact on cellular function.

Committee	Closed Committee - Engineering & Biological Systems (EBS)
Research Topics	Animal Health, Microbiology, Systems Biology, Technology and Methods Development
Research Priority	X – Research Priority information not available
Research Initiative	ANR-BBSRC SysBio (ANR-BBSRC SysBio) [2007]
Funding Scheme	X – not Funded via a specific Funding Scheme

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