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Grant: Research Tools and Instruments - Category 1 (<$150,000)

University of Manitoba

$136,935.00

Efficient Protein and Protein-Ligand complex characterization via SEC-MALS

EF 2013-14

Résumé
Research programs in the laboratories of the four applicants (Drs. Stetefeld, McKenna, Khajehpour and O'Neil) are focused on investigating a variety of interesting biological systems including integral membrane proteins with catalytic activities and integral membrane protein channels, a chlorophyll biosynthesis enzyme, monoclonal antibodies from llama, viral nucleic acid recognition proteins, a regulatory bacterial kinase and a transcription activator. The common feature that links each of these research groups is the structural and functional characterization of specific protein samples and their potential ligands to investigate their role in regulating the biological systems of interest. Rapid advances in the field of structural biology have allowed the research groups included in this proposal to determine high-resolution three-dimensional images of protein-ligand complexes, and begin to characterize their biochemical function and mechanism in terms of key molecular features that dictate the interaction. As an integral component of this strategy, light scattering approaches in combination with size exclusion chromatography that allow the absolute determination of molecular features of a protein in solution and the relevant protein-ligand complex have emerged as a central feature of protein structure/function research laboratories. The requested Size Exclusion Chromatography-Multiple Angle Light Scattering instrument (SEC-MALS) provides a valuable tool (i) to explore the absolute molecular mass information at every point of the size-separated sample, (ii) to identify protein and relevant protein-ligand complexes and their association state, (iii) to detect higher-order aggregates and protein conjugates, and (iv) to detect the molecular mass of the conjugates to rapidly and unambiguously determine stoichiometry. When combined with the already existing infrastructure accessible to our research groups, SEC-MALS provides a powerful means to analyze biomolecular interactions and to study molecular details of protein binding and protein stability. No SEC-MALS instrument is currently available in the Province of Manitoba. Therefore there is a clear and urgent need for the acquisition of this crucial piece of infrastructure.
Programme
Research Tools and Instruments - Category 1 (<$150,000)
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
458513-2014
Name nom
Stetefeld, JËrg
Department département
Chemistry
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2014
Award amount
136935
Program id
EQPEQ
Program name en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1102
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
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
5400
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Biochemistry
Research subject fr
Biochimie
Partie
1
Nb partie
1
Application title
Efficient Protein and Protein-Ligand complex characterization via SEC-MALS
Keyword
NSERC
Application summary
Research programs in the laboratories of the four applicants (Drs. Stetefeld, McKenna, Khajehpour and O'Neil) are focused on investigating a variety of interesting biological systems including integral membrane proteins with catalytic activities and integral membrane protein channels, a chlorophyll biosynthesis enzyme, monoclonal antibodies from llama, viral nucleic acid recognition proteins, a regulatory bacterial kinase and a transcription activator. The common feature that links each of these research groups is the structural and functional characterization of specific protein samples and their potential ligands to investigate their role in regulating the biological systems of interest. Rapid advances in the field of structural biology have allowed the research groups included in this proposal to determine high-resolution three-dimensional images of protein-ligand complexes, and begin to characterize their biochemical function and mechanism in terms of key molecular features that dictate the interaction. As an integral component of this strategy, light scattering approaches in combination with size exclusion chromatography that allow the absolute determination of molecular features of a protein in solution and the relevant protein-ligand complex have emerged as a central feature of protein structure/function research laboratories. The requested Size Exclusion Chromatography-Multiple Angle Light Scattering instrument (SEC-MALS) provides a valuable tool (i) to explore the absolute molecular mass information at every point of the size-separated sample, (ii) to identify protein and relevant protein-ligand complexes and their association state, (iii) to detect higher-order aggregates and protein conjugates, and (iv) to detect the molecular mass of the conjugates to rapidly and unambiguously determine stoichiometry. When combined with the already existing infrastructure accessible to our research groups, SEC-MALS provides a powerful means to analyze biomolecular interactions and to study molecular details of protein binding and protein stability. No SEC-MALS instrument is currently available in the Province of Manitoba. Therefore there is a clear and urgent need for the acquisition of this crucial piece of infrastructure.