Grant: Discovery Grants Program - Individual
York University
$105,000.00
Gas-phase chemistry of biological and metal-containing ions
EF 2009-10
Résumé
Explosive and significant advances in proteomics have been made possible by innovative technological breakthroughs and conceptual developments in biological mass spectrometry (MS). Two key technological areas that are the foundations of protein identification in MS are ion generation and collision-induced dissociation (CID) of peptides. Our proposed research continues to aim at better understanding the fundamentals of these reactions and processes, as well as the structures and energetics of the resulting ions. This knowledge is important for eventually more accurate and efficient protein sequencing and identification, especially in applications to discover and identify disease biomarkers. In particular, our objectives are to explore the structures, energetics, formation, and fragmentation chemistries of (i) molecular radical cations of oligopeptides; these ions differ from the neutral peptides by having one fewer electron, have structures and properties that are different from their protonated counterparts, and provide unique information when subject to CID-induced gas-phase microsequencing; and (ii) metalated peptides and ternary complexes; metalation imparts unique and interesting structures and chemistries to the peptides. The proposed investigations will be carried out by means of a combination of experiments, including tandem MS, threshold CID measurements, infrared multiple photon dissociation (IRMPD) spectroscopy, and DFT calculations. Tandem MS experiments will be conducted on prototype and/or commercially available mass spectrometers, including triple-quadrupole, linear ion trap, and three-dimensional ion trap. Threshold CID measurements will be conducted on a triple-quadrupole mass spectrometer fitted with a ring ion guide as q2. All of the above hardware is available in the applicant's laboratory at York University. IRMPD spectroscopic experiments will be performed in the Free Electron Laser for Infrared Experiments (FELIX) facility at the FOM-Institute for Plasma Physics "Rijnhuizen" in Nieuwegein, the Netherlands.
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
283305-2009
Name nom
Siu, Michael
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
2009
Competition year année de concours
2009
Award amount
105000
Program id
RGPIN
Program nane 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
26
Committee name en
Anal. & Phys. Chemistry
Committee name fr
Chimie analytique et physique
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
3505
Research subject group en
Analytical chemistry
Research subject group fr
Chimie analytique
Research subject en
Analytical spectroscopy
Research subject fr
Spectroscopie analytique
Partie
1
Nb partie
5
Application title
Gas-phase chemistry of biological and metal-containing ions
Keyword
NA
Application summary
Explosive and significant advances in proteomics have been made possible by innovative technological breakthroughs and conceptual developments in biological mass spectrometry (MS). Two key technological areas that are the foundations of protein identification in MS are ion generation and collision-induced dissociation (CID) of peptides. Our proposed research continues to aim at better understanding the fundamentals of these reactions and processes, as well as the structures and energetics of the resulting ions. This knowledge is important for eventually more accurate and efficient protein sequencing and identification, especially in applications to discover and identify disease biomarkers. In particular, our objectives are to explore the structures, energetics, formation, and fragmentation chemistries of (i) molecular radical cations of oligopeptides; these ions differ from the neutral peptides by having one fewer electron, have structures and properties that are different from their protonated counterparts, and provide unique information when subject to CID-induced gas-phase microsequencing; and (ii) metalated peptides and ternary complexes; metalation imparts unique and interesting structures and chemistries to the peptides. The proposed investigations will be carried out by means of a combination of experiments, including tandem MS, threshold CID measurements, infrared multiple photon dissociation (IRMPD) spectroscopy, and DFT calculations. Tandem MS experiments will be conducted on prototype and/or commercially available mass spectrometers, including triple-quadrupole, linear ion trap, and three-dimensional ion trap. Threshold CID measurements will be conducted on a triple-quadrupole mass spectrometer fitted with a ring ion guide as q2. All of the above hardware is available in the applicant's laboratory at York University. IRMPD spectroscopic experiments will be performed in the Free Electron Laser for Infrared Experiments (FELIX) facility at the FOM-Institute for Plasma Physics "Rijnhuizen" in Nieuwegein, the Netherlands.