Projects

MITOBIO

project name: Mitochondrial biogenesis: evolution of molecular machines.

initiating country: The European Union

Framework Programme: FP6       programme area: MC – Marie Curie Actions       contract type: MCOIF – Marie Curie Outgoing International Fellowship

contract/proposal/call number: 21898

status: active

start date: July 2006       duration: 36 months       projected finish date: July 2009

Keywords

keywords: Molecular evolution; Human parasitology; Protozoology

Project Budget

total budget: € 205,863

Participants

Note that the follow people may not represent the full extent of the consortium. FEAST has tried to identify the Australian participants, and their collaborators (or coordinator), within the project. Also note that Australian participation may not necessarily be on a formal level.

nameorganisationstate or country
UK Czech Republic
Mr Pavel DolezalThe University of Melbourne Czech Republic / VIC, Australia
The University of Melbourne VIC, Australia

Further information

summary:

The evolution of eukaryotes required creation of protein targeting pathways to ensure discrete populations of proteins could be sent into each compartment. Various compartments, such as mitochondria, plastids, the nucleus and peroxisomes are eukaryote-specific and building protein targeting pathways for these compartments depended on the de novo creation of specific molecular machines. The purpose of this project is to search for and characterize components of equivalent molecular machines in the membranes of the mitochondria-related organelles found in some of the ancient protist species that represent significant parasites of humans. Candidates of TOM, TIM and PAM complex components involved in protein import into mitochondria-related organelles of Giardia intestinalis Entamoeba histolytica and Trichomonas vaginalis will be characterized. Our aim is to use comparative analyses to understand how a defined set of such molecular machines were created, and mechanistic details of how they provide their function in protein transport across membranes in each of the organisms in which they are found.

Source: European commission