Award details

Intracellular distribution of Cu(I): De-regulation & exploitation in pathogen-control.

Reference	BB/H011110/2
Principal Investigator / Supervisor	Professor Nigel Robinson
Co-Investigators / Co-Supervisors	Dr Julian Rutherford
Institution	Durham University
Department	Biological and Biomedical Sciences
Funding type	Research
Value (£)	310,806
Status	Completed
Type	Research Grant
Start date	30/06/2011
End date	29/12/2013
Duration	30 months

Abstract

Firstly, reports in the literature suggest that plasma membrane copper importers Ctr1, Ctr3 supply copper to the copper metallochaperones CCS and Atx1 while vacuole export via Ctr2 contributes only modestly. These published data imply that the pool of copper for SOD1 and the trans-Golgi network mostly originates from cell surface importers rather than from exporters of vacuole copper. Secondly, the immediate source of copper for Cox17, hence Sco1 and Sco2, and hence the copper A and B sites of cytochrome oxidase, appears to be a low molecular weight copper complex which is present in the mitochondrial matrix, from yeast to humans. The source of copper for the low molecular weight mitochondrial copper complex remains to be defined. Finally, the sources of copper for the two nuclear copper detectors, Ace1 and Mac1, are unclear although the detection of copper by Mac1 is now known to depend upon the catalytic activity of a nuclear pool of SOD1. Treatment of S. cerevisiae with a copper-chelating fungicide generated by chemists at Syngenta prevents growth on a non-fermentable carbon source, lactate, but growth is restored by the addition of 2 percent glucose, indicative of a loss of activity of cytochrome oxidase. This is suggestive of a loss of copper supply via the Cox17 route. In seeming conflict with these data, beta-galactosidase activity driven by a cup1 promoter-lacZ fusion was concurrently greatly enhanced and S1 nuclease protection assays confirm greatly enhanced accumulation of cup1 transcripts. This is suggestive of enhanced copper supply to Ace1. The effects of the chelator on the intracellular distribution of copper will be determined. This is an opportunity to understand how copper is targeted to its different intracellular destinations.

Summary

Copper is widely used in the agrochemical industry as a fungicide and Syngenta are investigating new copper based formulations with greater efficacy and/or requiring lower environmental copper input. Fortuitously, one of the Cu(I)-chelator compounds produced by synthetic chemists at Syngenta appears to de-regulate copper homeostasis in S. cereviasiae, as well as inhibiting growth of several pathogenic fungi. Via such de-regulation, this Cu(I)-chelator has the potential to provide insight into the pathways that deliver this metal to its destinations inside living cells. Specifically, preliminary data suggest that the sources of copper for each copper delivery pathway are not identical. This is a rare opportunity to explore fundamental questions at the heart of the cell biology of metals, while simultaneously tackling issues of direct relevance to an agrochemical company. Syngenta would like to understand the biochemical basis via which the Cu(I)-chelator acts if it is to be pursued commercially, and the 'Metals in Cells Group' at Newcastle University are eager to use the Cu(I)-chelator to explore how copper is correctly targeted inside cells. Copper is essential for enzymes such as cytochrome oxidase, superoxide dismutase 1, and (in plants) plastocyanin. Some metals, especially copper, have a tendency to form much tighter complexes with proteins than do others. Cells must maintain exceptionally low buffered cytosolic concentrations of copper in order to minimise the mis-population of proteins that require the less competitive metals. Copper must also be tightly controlled due to its propensity to engage in redox chemistry such as the Fenton reaction which generates deadly hydroxyl radicals. To avoid copper-release in the cytosol it is supplied to copper requiring proteins under kinetic control, meaning that copper is delivered to its correct destinations by specific 'copper metallochaperones'. The metal is passed from the copper metallochaperones to their partnersby sequences of ligand-exchange reactions. In most eukaryotic cells, including fungi, these include copper metallochaperones for cytochrome oxidase in mitochondria, one for superoxide dismutase 1 in the cytosol and finally one for the trans-Golgi network. However, it is unclear where the copper metallochaperones themselves obtain copper and it is also unclear how the routing of copper to these different cellular destinations is prioritised, especially when copper is in short supply. These are fundamental unknowns in regard to copper homeostasis in all organisms; plants, fungi, bacteria and animals including humans. An intriguing hypothesis is that the copper chaperones for cytochrome oxidase have access to copper released at cuproprotein turnover, while those for SOD1 and for the trans-Golgi network predominantly have access to newly imported copper. This would ensure that as copper levels decline the metal ions become predominantly routed to a most vital intracellular destination, namely cytochrome oxidase. Fungal cells treated with the Cu(I)-chelator generated by Syngenta chemists appear to detect high intracellular copper concentrations by switching on expression of (metallothionein Cup1-1 and Cup1-2) genes whose products mop up surplus copper. However, the treated cells concurrently exhibit phenotypes consistent with insufficient copper reaching cytochrome oxidase. A goal of this programme is to measure the respective cupro-enzyme activities and quantify the amounts of copper reaching the different destinations. This will establish if there are distinct sources of copper for the different copper delivery pathways.

Impact Summary

This programme is an IPA partly funded by Syngenta. Thus, Syngenta are the most immediate industrial beneficiaries (other forms of impact are described in the full impact plan). Syngenta have crop treatments on the market which use copper, or metal-chelators, as the active ingredients. Following an initial approach from Syngenta in late 2008, a joint consultancy agreement was negotiated which has already generated some income supporting research in the Robinson lab. The consultancy agreement is ongoing and will be extended coincident with the award of this grant. A pre-proposal version of this application was approved by an internal board within Syngenta early in 2009, giving authorisation for this IPA application to BBSRC. Syngenta will crucially provide the copper-chelator compounds required for this work, under a strict collaborative agreement. Throughout the grant there will be regular meetings either at Syngenta or in Newcastle (in preparation for this application Andy Corran has flown to Newcastle twice already in 2009 and Robinson has travelled to Jealotts Hill). Such regular meetings will ensure that discoveries with industrial impact are exploited in the swiftest possible manner.

Committee	Research Committee B (Plants, microbes, food & sustainability)
Research Topics	Microbiology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	Industrial Partnership Award (IPA)

Associated awards:

BB/H011110/1 Intracellular distribution of Cu(I): De-regulation & exploitation in pathogen-control.

I accept the terms and conditions of use (opens in new window)

export PDF file

back to list new search