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Grant: Discovery Grants Program - Individual

Brock University

$42,000.00

Proteomes of proteoforms - improving routine top-down proteomic analyses

EF 2019-20

Résumé
Proteins drive cellular processesthey are the molecular workhorses of life. The large-scale analysis of proteins (Proteomics) is a cornerstone of research supporting a range of studies related, for example, to environmental, agricultural, health and industrial research. ***A given protein exists as multiple molecular species (proteoforms) because of specific chemical alterations called post-translational modifications (PTM) that tune its actions. To analyze the proteins in a biological sample (the proteome), we must assess proteoforms effectively; yet, commonly applied proteome analyses do not routinely do this, but use random amino acid sequencing to catalog proteins possibly present. We are further developing top-down' analyses by two-dimensional gel electrophoresis (2DE) to resolve, in a single gel, thousands of proteoforms that can then be identified by amino acid sequencing using mass spectrometry (MS). We are recognized for the systematic optimization of 2DE for quantitative proteomics, including refinement of a highly sensitive, cost-effective stain (cCBB) for protein detection.***With attention to proteoforms, our program centers on the following objectives over the next five years: ***1. To build on the superior detection sensitivity of cCBB by combining it with other stains, and synthesize and test chemical variants of cCBB, in part by defining how another sensitive stain binds differently to proteins and targeting modifications to cCBB accordingly.***2. To identify proteoforms they are cut from 2D gels, treated with specific enzymes, and the resulting peptides sequenced by MS. The most common protocol results in lost information. We will systematically refine the procedure to ensure the best MS data and thus proteoform identifications. ***3. To introduce a routine third separation step after 2DE, ensuring the best possible resolution and thus proteoform identifications by subsequent peptide sequencing. ***4. To prototype new imaging instrumentation for the highest sensitivity in-gel detection of resolved proteoforms, enabling extraction of the most information per analysis and identification of those proteoforms critical to the biology under study.***5. To resolve proteomes in ultrathin (~0.2mm) 2D gels adapting industry standard materials, markedly reducing total protein per analysis and improving detection sensitivity, ***Overall, our research program will improve proteoform resolution, detection, and identification, largely by high quality, low-cost refinements that enable the widespread use of high-calibre proteomic analyses. We will provide cutting-edge training and career development for the next generations of leaders in research, healthcare, and industry. The results will be of global interest and benefit across fundamental and applied research. Multiple research areas and industry will be impacted. This is the conception of fundamental research having the broadest potential ramifications. **
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2019-04324
Name nom
Coorssen, Jens
Department département
Health Sciences
Organization id
22
Institution établissement
Brock University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2019
Award amount
42000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5403
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Proteins and peptides, amino acids
Research subject fr
Protéines et peptides, acides aminés
Installment
inst:1 - 5
Partie
1
Nb partie
5
Application title
Proteomes of proteoforms - improving routine top-down proteomic analyses
Keyword
NSERC
Application summary
Proteins drive cellular processesthey are the molecular workhorses of life. The large-scale analysis of proteins (Proteomics) is a cornerstone of research supporting a range of studies related, for example, to environmental, agricultural, health and industrial research. ***A given protein exists as multiple molecular species (proteoforms) because of specific chemical alterations called post-translational modifications (PTM) that tune its actions. To analyze the proteins in a biological sample (the proteome), we must assess proteoforms effectively; yet, commonly applied proteome analyses do not routinely do this, but use random amino acid sequencing to catalog proteins possibly present. We are further developing top-down' analyses by two-dimensional gel electrophoresis (2DE) to resolve, in a single gel, thousands of proteoforms that can then be identified by amino acid sequencing using mass spectrometry (MS). We are recognized for the systematic optimization of 2DE for quantitative proteomics, including refinement of a highly sensitive, cost-effective stain (cCBB) for protein detection.***With attention to proteoforms, our program centers on the following objectives over the next five years: ***1. To build on the superior detection sensitivity of cCBB by combining it with other stains, and synthesize and test chemical variants of cCBB, in part by defining how another sensitive stain binds differently to proteins and targeting modifications to cCBB accordingly.***2. To identify proteoforms they are cut from 2D gels, treated with specific enzymes, and the resulting peptides sequenced by MS. The most common protocol results in lost information. We will systematically refine the procedure to ensure the best MS data and thus proteoform identifications. ***3. To introduce a routine third separation step after 2DE, ensuring the best possible resolution and thus proteoform identifications by subsequent peptide sequencing. ***4. To prototype new imaging instrumentation for the highest sensitivity in-gel detection of resolved proteoforms, enabling extraction of the most information per analysis and identification of those proteoforms critical to the biology under study.***5. To resolve proteomes in ultrathin (~0.2mm) 2D gels adapting industry standard materials, markedly reducing total protein per analysis and improving detection sensitivity, ***Overall, our research program will improve proteoform resolution, detection, and identification, largely by high quality, low-cost refinements that enable the widespread use of high-calibre proteomic analyses. We will provide cutting-edge training and career development for the next generations of leaders in research, healthcare, and industry. The results will be of global interest and benefit across fundamental and applied research. Multiple research areas and industry will be impacted. This is the conception of fundamental research having the broadest potential ramifications. **