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Structure-Function Analysis of a Key Mitochondrial PrxIII Antioxidant Defence Pathway: Roles in Antioxidant Defence & Chaperone-Mediated Protection

Reference	BB/F001851/1
Principal Investigator / Supervisor	Professor John Lindsay
Co-Investigators / Co-Supervisors	Professor Neil William Isaacs
Institution	University of Glasgow
Department	Institute of Biomedical & Life Sciences
Funding type	Research
Value (£)	474,365
Status	Completed
Type	Research Grant
Start date	01/02/2008
End date	28/02/2011
Duration	37 months

Abstract

Mitochondria are the main intracellular sites of respiration producing reactive oxygen species (ROS) as toxic by-products. Key antioxidant enzymes, the peroxiredoxins, are emerging as critical regulators of intracellular H2O2 levels where they are implicated both in tissue protection against oxidative stress and in cellular responses via H2O2-mediated signalling pathways. We have purified and reconstituted, the major mitochondrial antioxidant defence pathway involving peroxiredoxin III (PrxIII), a thioredoxin-dependent peroxidase and its cognate partners, thioredoxin and thioredoxin reductase. Our 3.3Å structure for C168S PrxIII shows its presence as 2 interlinked, dodecameric toroids, a protein catenane. Several key features of PrxIII have also been identified including its sensitivity to overoxidation and factors/ mutations influencing dodecamer-dimer interconversion and PrxIII activity. A direct physical/ functional interaction has also been established with the pyruvate and 2-oxoglutarate dehydrogenase complexes that have pivotal roles in carbohydrate utilisation and are prime targets for oxidative damage. Key goals are: (a)(i) to determine the structure of oxidised PrxIII for comparison with the catenated (reduced) state (C168S PrxIII); (ii) to conduct structure/ activity studies on a series of PrxIII variants, namely His-tagged wild-type enzyme and S78D, S78V, S78I mutants that are defective in peroxidase activity and dodecamer-dimer interconversion. (b) to investigate if overoxidation/ heat shock treatment of PrxIII (and various mutants) leads to formation of higher mol wt complexes with novel chaperone-like properties. (c) to investigate physical/ functional links between PDC, OGDC and PrxIII in detail and to identify additional candidate mitochondrial proteins that are susceptible to oxidative damage. (d) to analyse the effects of overexpression of various types of defective Prx mutants on mitochondrial integrity and cell viability.

Summary

Mitochondria are the powerhouses of cells liberating energy from the breakdown of the major fuel molecules, namely carbohydrates, fats and proteins as the 'high-energy' chemical ATP. ATP is the universal 'energy currency' of all living organisms where it is required for powering all the normal bodily activities associated with life itself. Mitochondria are also the principal sites of intracellular respiration (oxygen consumption) where reactive oxygen species (ROS), in essence partially-reduced forms of oxygen, so-called superoxide anions, hydroxyl radicals and hydrogen peroxide, are also produced continuously as naturally-occurring, toxic by-products of respiration that are potentially very damaging to tissues. As a result, organisms have evolved an integrated network of enzyme-based, antioxidant defence systems to ensure the rapid removal of these potentially harmful species. However, oxidative stress can occur when there is an imbalance in the production of ROS that can temporarily overwhelm cellular antioxidant defences. As this is a potentially lethal event, cells must respond appropriately to minimise the extent of irreversible damage wherever possible and ensure their ultimate survival. Recent studies on a newly-emerging group of antioxidant enzymes, the peroxiredoxins (Prxs) have revealed that they serve as critical regulators of intracellular hydrogen peroxide concentrations with dual roles in tissue protection and hydrogen peroxide-mediated cell signalling responses to elevated ROS levels. In our laboratory, we have recently reconstituted the main human mitochondrial peroxiredoxin pathway in vitro and elucidated some its novel properties by producing and purifying its its 3 constituent enzymes in bacteria permitting detailed investigation of its role in antioxidant defence. A unique 3D structure has also been determined for its principal component, PrxIII that directly reduces hydrogen peroxide to water with the aid of its partner proteins, thioredoxin and thioredoxin reductase. PrxIII has a remarkable subunit organisation comprising two mechanically-interlocked rings, each assembled from 12 identical protein subunits, one of only two known examples of a so-called protein catenane. Moreover, PrxIII can exist in various states of assembly (oligomeric states) under different conditions. These include basic dimeric units (2 subunits), single dodecameric rings, 2-ring catenanes and long, regular filamentous structures containing multiple rings. We now wish to investigate the central biological importance of this key antioxidant defence system in greater detail and the relevance of the presence of multiple structural forms of Prx III in the regulation of pathway activity as oxidative stress is implicated as a major causative factor in a range of human diseases including cardiovascular disease, cancer, diabetes and neurodegenerative disorders. Our research will also focus on how the PrxIII pathway interacts with and protects a vital group of mitochondrial multienzyme complexes involved in degrading the major fuel molecules; on identifying other key mitochondrial proteins that are susceptible to damage under conditions of oxidative stress; and on elucidating how defective functioning of PrxIII in vivo affects mitochondrial integrity, energy production and cell viability.

Committee	Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics	Ageing, Structural Biology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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