Award details

SCOTSMAN (SCOttish Trace element Speciation & Metabolomics Analytical Network) - a request for a high resolution ICP-MS to accomplish HPLC-ES-qTOFMS

Reference	BB/F011687/1
Principal Investigator / Supervisor	Professor Jorg Feldmann
Co-Investigators / Co-Supervisors	Professor Ian Booth, Professor Marcel Jaspars, Professor Andrew Meharg
Institution	University of Aberdeen
Department	Chemistry
Funding type	Research
Value (£)	161,594
Status	Completed
Type	Research Grant
Start date	03/10/2008
End date	02/10/2009
Duration	12 months

Abstract

The technology of high resolution elemental mass spectrometry has matured over the last decade but its potential in life sciences has not been recognized so far. Although quadrupole ICP-MS have been used for decades as detectors for HPLC in order to determine low molecular mass metal species. But it was only when this set-up was combined directly with electrospray MS, that it became a powerful tool for the identification and quantification of biomolecules. However, this set-up has also shown its limitations, since the quadrupole ICPMS are not capable of determining the more common hetero-elements in bioligands such as phosphorous and sulphur. Although the technology is capable of detecting those non-metals with high sensitivity and interference-free by using double focussing sector field ICP-MS, it has never been used in the combination with HPLC and electrospray mass spectrometry. We propose to combine the requested high resolution ICPMS (Element 2) with an ES-qTOFMS for measuring the accurate mass or molecular formula of an eluting compound directly when online coupled to HPLC and to quantify the compound by utilising the independence of plasma responses of different species containing one hetero-element. Here we capitalize on our experience in combining dual mass spectrometry facilities for liquid chromatography in order to identify and quantify unstable intermediates and compounds of low abundance in cell extracts. This set-up makes it possible to identify new biomolecules and quantify known species of importance in a mixture of hundreds of untagged molecules in the extracts. In particular the quantification of post translational modification of proteins by phosphorylation and sulphurylation may become a routine technique.

Summary

Medical diagnosis and the resulting treatment will improve the results significantly when a more personalized system for health assessment is implemented. This can be achieved by providing detailed information about the metabolic status of individuals. The use of metabolomic data to predict the health trajectories of individuals will require bioinformatic tools and quantitative reference databases. For example protein phosphorylation is probably the most important regulatory event in eukaryotes. Many enzymes and receptors are switched 'on' or 'off' by phosphorylation and dephosphorylation. Antibodies can be used as powerful tools to detect whether a protein is phosphorylated at any particular site. Such antibodies are called phospho-specific antibodies; hundreds of such antibodies are now available. They are becoming critical reagents both for basic research and for clinical diagnosis. Approaches to identify and more importantly quantify phosphorylated proteins, like mass spectrometry-based proteomics, are becoming increasingly important for the systematic analysis of complex phosphorylation networks. However, most of them lack the ability to identify the phosphorylation status rapidly and accurately. Furthermore, other post translational modification such as sulphurylation and the redox status of translational proteins and selenoproteins could give vital information about the metabolic status of an individual. Two challenges lie ahead for the bioanalytical community; the separation of the complex mixtures of metabolites, peptides and proteins and their quantitative determination. Most methods can only cover one of the challenges. Here, with this proposal, we seek funding to complete the world-wide unique set-up the SCOttish Trace element Speciation & Metabolomics Analytical Network (SCOTSMAN), a new combination of chromatography and/or electrophoresis and dual mass spectrometry to develop a rapid separation technique which is capable of online identification andquantification of metabolites and proteins which have been labelled or tagged in a complex matrix of organic compounds which do not contain an hetero-element. Hence, this method is able to pick out the needles in the haystack. This set-up will be able to quantify biomolecules containing a hetero-element such as phosphorous or sulphur or metals and metalloids such as copper, selenium and arsenic. Using element-specific detection coupled with high resolution mass separation, the requested instrument is capable of quantifying the compounds at ultra-trace level which is relevant for background studies and non diseased individuals. Since the instrument response is not dependant on the compound itself, it can be used to quantify the element in the introduced sample without having the exact compound as a standard. If that analyser is now coupled to a separation method online, the unambiguous quantification of the compound carrying the tag or label can be done directly. When identification of certain metabolites is of importance, the second complementary molecular mass analyser (already in place) will provide accurate data on the mass of the molecule simultaneously. This information is vital to deduce molecular formula. Altogether this proposal, supported by the manufacturer and a charity organisation has an extremely good add on value, since the requested instrument will be coupled directly with additional complementary mass analyser with similar calibre to built this unique analytical set-up for biologists, plant physiologists, microbiologists, researcher interested in systems biology and pharmacologists.

Committee	Closed Committee - Plant & Microbial Sciences (PMS)
Research Topics	Technology and Methods Development
Research Priority	X – Research Priority information not available
Research Initiative	Research Equipment Initiative 2007 (RE7) [2007]
Funding Scheme	X – not Funded via a specific Funding Scheme

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

export PDF file

back to list new search