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

York University

$93,751.00

Multi-angle light scattering instumentation for macromolecule characterization

EF 2007-08

Résumé
Nanotechnology has progressed significantly over the past decade, based largely on the unique properties of carbon nanotubes. The development of biologically relevant nanomachines and their building blocks has, in general, focused on the addition of biological functionality to carbon nanotube scaffolds. However, despite the unique chemical properties of carbon nanotubes, their use in biological systems remains limited due to issues with direct and/or indirect toxicity. My research program focuses on identifying and engineering protein-based systems as an alternative approach to the development of biologically accepted nanostructures. This method has several advantages over the carbon nanotube adaptation, including access to modern protein engineering tools and the ready biological acceptance of a structure that is itself biotic in origin.  I recently discovered the assembly of a protein nanotube from an engineered form of the type IV pilin protein from the bacteria Pseudomonas aeruginosa, which represents the first instance of the controlled generation of a nanotube from a soluble monomeric protein under physiological conditions. The current proposal aims at characterizing the assembly and structure of these novel protein nanotubes, adding specific functionalities to the protein nanotubes through protein engineering, and examining the oligomerization of protein nanotubes on conducting and semi-conducting surfaces. A central component to the characterization of protein nanotube oligomerization is the study of the hydrodynamic properties of the pilin protein during oligomerization into protein nanotubes. These studies will greatly increase our understanding of the assembly of these unique nanostructures and provide a significant step forward in the development of protein nanotubes for bionanotechnology applications.
Programme
Research Tools and Instruments - Category 1 (<$150,000)
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
359367-2008
Name nom
Audette, Gerald
Department département
Chemistry
Organization id
38
Institution établissement
York University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2008
Award amount
93751
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
24
Committee name en
Inorganic & Organic Chemistry
Committee name fr
Chimie inorg. et org.
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
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
Multi-angle light scattering instumentation for macromolecule characterization
Keyword
NA
Application summary
Nanotechnology has progressed significantly over the past decade, based largely on the unique properties of carbon nanotubes. The development of biologically relevant nanomachines and their building blocks has, in general, focused on the addition of biological functionality to carbon nanotube scaffolds. However, despite the unique chemical properties of carbon nanotubes, their use in biological systems remains limited due to issues with direct and/or indirect toxicity. My research program focuses on identifying and engineering protein-based systems as an alternative approach to the development of biologically accepted nanostructures. This method has several advantages over the carbon nanotube adaptation, including access to modern protein engineering tools and the ready biological acceptance of a structure that is itself biotic in origin.  I recently discovered the assembly of a protein nanotube from an engineered form of the type IV pilin protein from the bacteria Pseudomonas aeruginosa, which represents the first instance of the controlled generation of a nanotube from a soluble monomeric protein under physiological conditions. The current proposal aims at characterizing the assembly and structure of these novel protein nanotubes, adding specific functionalities to the protein nanotubes through protein engineering, and examining the oligomerization of protein nanotubes on conducting and semi-conducting surfaces. A central component to the characterization of protein nanotube oligomerization is the study of the hydrodynamic properties of the pilin protein during oligomerization into protein nanotubes. These studies will greatly increase our understanding of the assembly of these unique nanostructures and provide a significant step forward in the development of protein nanotubes for bionanotechnology applications.