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An Integrated Open Source Software Resource for Quantitative Proteomics

Bbsrc · United Kingdom government procurement

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Opportunity Overview

In a scientific sense, a living system such as a plant, animal, organ or cell can be considered to be a complex machine. The basic components that make up this machine are molecules, of which there are several main types - genes, proteins and metabolites. To understand how these molecules work together to produce the complex living systems that we see around us we need to have analytical methods capable of detecting and quantifying these molecules. This proposal deals with one aspect of this analysis - proteomics - the science of identifying and quantifying proteins. The most popular approach in proteomics is to simplify a sample by separating all the proteins, digesting those proteins with an enzyme into much smaller components (peptides) and then analysing all these peptides with mass spectrometry (MS). Identification of proteins can then be carried out by computational analysis of the mass spectrum acquired from each peptide - peptides are usually mapped to proteins by comparison of observed spectra to those in a database. Protein quantity is typically calculated from mass spectral peak intensities, or by simply considering how many peptides have been observed from each protein. Within this general analytical schema there are a great many variations according to the laboratory that is doing the analysis, the samples being analysed, or the overall aim of the experiment. Factors that may differ between experimental protocols include the protein separation method (some people use gels, others liquid chromatography), different types of mass spectrometry, different search databases (some are simulated from protein sequences, others are libraries of experimentally acquired spectra), and different methods of quantitation (for instance there are various methods of labelling which are used to distinguish peptides from different samples during the analysis). This plethora of quantitative proteomic methods has two major disadvantages for proteomics practitioners. Firstly,...

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Solicitation Details

Issuing agencyBbsrc
CountryUnited Kingdom
CategorySoftware Development
Response dueNot specified / rolling
StatusActive - open for responses
Official sourceView original notice

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