Grant: Discovery Grants Program - Individual
Saint Mary's University
$27,000.00
Probing membrane transport using plasmonic nanoarrays engineered for surface-enhanced spectroscopies
EF 2010-11
Résumé
This research proposal seeks to develop a novel tool for the investigation of electric field-driven membrane transport phenomena, based on nanoparticle plasmonics and surface-enhanced vibrational spectroscopies. This research will be utilized to probe a variety of voltage-gated membrane transport processes, with an emphasis on biomimetic membrane systems. Of particular interest is the degree to which protein aggregates, such as amyloids, interact with biomembrane systems, and what kind of channels are formed as a result of this interaction. Other systems of interest include the transduction of particular protein toxins across membrane systems, and a better understanding of small molecule permeation through pre-existing protein transmembrane channels.
Nanoarray electrodes composed of metal nanoparticles will be designed and engineered to allow for maximum signal attainment in various surface-enhanced spectroscopies, including surface-enhanced Raman spectroscopy (SERS) and surface-enhanced infrared reflection absorption spectroscopy (SEIRRAS). The very short decay lengths (i.e. < 10 nm for SERS) of the enhanced electric field generated by metal nanostructures makes it possible to record signal from only those species which cross the membrane and arrive at the nanostructured electrode surface, providing the basis of a new methodology for studying membrane transport phenomena. Of particular value is that this approach does not require special labels or probe molecules, and studies can be done in a real time, in situ manner.
This research will contribute to our understanding of the design and development of plasmonic nanoarray electrodes, and will enhance our knowledge of voltage-gated membrane transport, particularly with respect to the interaction between aggregated protein and cellular membranes. Findings from such research will be critical to the understanding of disease processes caused by protein aggregates, and may highlight future avenues of disease research.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Nova Scotia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
386427-2010
Name nom
Brosseau, Christa
Department département
Chemistry
Organization id
85
Institution établissement
Saint Mary's University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2010
Award amount
27000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
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
3402
Research subject group en
Physical chemistry
Research subject group fr
Chimie physique
Research subject en
Surface and interfacial chemistry
Research subject fr
Chimie des surfaces et des interfaces
Partie
1
Nb partie
5
Application title
Probing membrane transport using plasmonic nanoarrays engineered for surface-enhanced spectroscopies
Keyword
NSERC
Application summary
This research proposal seeks to develop a novel tool for the investigation of electric field-driven membrane transport phenomena, based on nanoparticle plasmonics and surface-enhanced vibrational spectroscopies. This research will be utilized to probe a variety of voltage-gated membrane transport processes, with an emphasis on biomimetic membrane systems. Of particular interest is the degree to which protein aggregates, such as amyloids, interact with biomembrane systems, and what kind of channels are formed as a result of this interaction. Other systems of interest include the transduction of particular protein toxins across membrane systems, and a better understanding of small molecule permeation through pre-existing protein transmembrane channels.
Nanoarray electrodes composed of metal nanoparticles will be designed and engineered to allow for maximum signal attainment in various surface-enhanced spectroscopies, including surface-enhanced Raman spectroscopy (SERS) and surface-enhanced infrared reflection absorption spectroscopy (SEIRRAS). The very short decay lengths (i.e. < 10 nm for SERS) of the enhanced electric field generated by metal nanostructures makes it possible to record signal from only those species which cross the membrane and arrive at the nanostructured electrode surface, providing the basis of a new methodology for studying membrane transport phenomena. Of particular value is that this approach does not require special labels or probe molecules, and studies can be done in a real time, in situ manner.
This research will contribute to our understanding of the design and development of plasmonic nanoarray electrodes, and will enhance our knowledge of voltage-gated membrane transport, particularly with respect to the interaction between aggregated protein and cellular membranes. Findings from such research will be critical to the understanding of disease processes caused by protein aggregates, and may highlight future avenues of disease research.