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Grant: Collaborative Research and Development Grants

University of Manitoba

$78,260.00

Enhancing quantitative proteomics through the accurate prediction of retention time of peptides labeled with tandem mass tags

EF 2019-20

Résumé
The combination of liquid chromatography and mass spectrometry (LC-MS) for the analysis of proteins and peptides has become an indispensible component of analytical science applied to human health, agriculture, energy, and environmental studies. The mass-spectrometry component of this technique has been the primary focus of instrument development. At the same time, the LC component of the system can provide very valuable information, given the ability to predict the retention properties of analyzed molecules. Overall this will make LC-MS a ""double-edged sword"", where the outcomes from both methods can be used to improve the analysis output. My laboratory has been the leader in the peptide retention time prediction field for more than a decade. Our Sequence-Specific Retention Calculator (SSRCalc) model has become a benchmark tool in the field, attracting attention both from the proteomic/chromatographic community and from major vendors of proteomics equipment and software. In this proposal we aim to join our expertise with the leading provider of LC-MS proteomic systems, Thermo Fisher Scientific (TFS).One of the key applications developed by TFS targets protein quantitation through peptide labeling with tandem-mass tag (TMT) reagents, followed by LC-MS analysis. Chromatographic properties of the labeled peptides are significantly different from their non-labeled counterparts, thus limiting application of current retention prediction algorithms, including SSRCalc. Another improvement introduced by TFS is the use of ultra small chromatographic particles and higher separation temperature to reduce column backpressure. This alters the accuracy prediction models, too. The focus of this Collaborative Research and Development Grant is to extend the SSRCalc prediction methodology into peptides labeled with TMT and separations using various temperatures. This will result in the new generation of our model - Universal Sequence-Specific Retention Calculator (USSRCalc) - as it will cover wider range of chromatographic conditions with unmatched performance, and will lead to development of simplified quantitation protocols for clinical proteomics.
Programme
Collaborative Research and Development Grants
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
520351-2017
Name nom
Krokhin, Oleg
Department département
Internal Medicine
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2017
Award amount
78260
Program id
CRDPJ
Program name en
Collaborative Research and Development Grants
Program name fr
Subventions de recherche et développement coopérative
Group en
RESEARCH PARTNERSHIPS
Group fr
PARTENARIATS DE RECHERCHE
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
1101
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Human health (including medically-related psychological research)
Area of application fr
Santé publique (y compris recherche psychologique liée à la médecine)
Research subject code
3504
Research subject group en
Analytical chemistry
Research subject group fr
Chimie analytique
Research subject en
Bioanalytical chemistry
Research subject fr
Chimie bioanalytique
Installment
inst:2 - 2
Partie
2
Nb partie
2
Application title
Enhancing quantitative proteomics through the accurate prediction of retention time of peptides labeled with tandem mass tags
Keyword
NSERC
Application summary
The combination of liquid chromatography and mass spectrometry (LC-MS) for the analysis of proteins and peptides has become an indispensible component of analytical science applied to human health, agriculture, energy, and environmental studies. The mass-spectrometry component of this technique has been the primary focus of instrument development. At the same time, the LC component of the system can provide very valuable information, given the ability to predict the retention properties of analyzed molecules. Overall this will make LC-MS a ""double-edged sword"", where the outcomes from both methods can be used to improve the analysis output. My laboratory has been the leader in the peptide retention time prediction field for more than a decade. Our Sequence-Specific Retention Calculator (SSRCalc) model has become a benchmark tool in the field, attracting attention both from the proteomic/chromatographic community and from major vendors of proteomics equipment and software. In this proposal we aim to join our expertise with the leading provider of LC-MS proteomic systems, Thermo Fisher Scientific (TFS).One of the key applications developed by TFS targets protein quantitation through peptide labeling with tandem-mass tag (TMT) reagents, followed by LC-MS analysis. Chromatographic properties of the labeled peptides are significantly different from their non-labeled counterparts, thus limiting application of current retention prediction algorithms, including SSRCalc. Another improvement introduced by TFS is the use of ultra small chromatographic particles and higher separation temperature to reduce column backpressure. This alters the accuracy prediction models, too. The focus of this Collaborative Research and Development Grant is to extend the SSRCalc prediction methodology into peptides labeled with TMT and separations using various temperatures. This will result in the new generation of our model - Universal Sequence-Specific Retention Calculator (USSRCalc) - as it will cover wider range of chromatographic conditions with unmatched performance, and will lead to development of simplified quantitation protocols for clinical proteomics.