Spelling suggestions: "subject:"eharge 1detection mass spectrometry"" "subject:"eharge 1detection mass pectrometry""
1 |
Charge Detection Mass Spectrometry Using Printed Circuit Board Arrays for the Analysis of Microparticles in the Martian AtmosphereGustafson, Elaura LuAnne 19 September 2022 (has links)
Charge detection mass spectrometry (CDMS) is a single particle technique capable of simultaneously measuring charge and mass-to-charge ratios for individual ions or particles. The linear array CDMS design theoretically has no upper mass limit and is therefore a choice method for the analysis of high mass and heterogeneous samples, such as dust microparticles in the Martian atmosphere. This dissertation describes the development of a novel charge detection mass spectrometer made of printed circuit boards (PCB) for the analysis of dust microparticles in the Martian atmosphere. Development of this device has required investigations in analysis methods and the engineering design of both the PCB device and the vacuum chamber system used in laboratory experiments. Accurate velocity analysis is crucial in determining correct particle mass in linear array CDMS. By combining the Shockley-Ramo theorem–which allows for the calculation of instantaneous image current for a system of electrodes when a point charge passes them–and SIMION ion optics simulations effective electrode length can be determined for any given charge detector geometry and aid in charge detector engineering and design process. Applying these simulation results to experimental data yields velocity agreement for a PCB charge detector within 0.44% RSD. The novel PCB CDMS device was demonstrated for the analysis of multiple types of microparticles of varying size and charge similar to that expected of atmospheric Mars dust. This device is able to measure particle charge above 1,500 elementary charges of either polarity. Simulations show that for microparticles having a size and density close to that which is expected for Mars dust, the device is able to ideally measure the mass of particles ranging from 0.2–2.5 μm in diameter, providing broad coverage of particles too small to be observed by optical scattering and other techniques that have been previously used on Mars.
|
2 |
Coupling Laser with Mass Spectrometry for Biomolecules Characterization : From Peptides towards Protein Fibrils / Couplage entre spectrométrie de masse et spectroscopie laser pour la caractérisation de biomolécules : des petits peptides modèles à de très gros assemblages protéiquesHalim, Mohammad Abdul 14 June 2017 (has links)
La spectrométrie de masse est devenue un outil indispensable pour la recherche en protéomique, notamment grâce au développement récent de nouveaux spectromètres de masse comme l’Orbitrap et de nouvelles méthodes de dissociation. La stratégie « bottom-up » (analyse des mélanges de peptides protéolytiques) est la plus utilisée par son efficacement et sa simplicité par rapport à la stratégie top-down (analyse des peptides plus longs ou des protéines intactes), mais cette dernière permet une caractérisation plus complète des isoformes de protéines et des modifications post-traductionnelles.Les méthodes de dissociation utilisant des photons, comme la photodissociation dans le domaine ultra-violet (UVPD) et la dissociation multiphotonique infrarouge (IRMPD), ont reçu une grande attention comme approches alternatives aux méthodes de dissociation par collision. L'absorption du photon UV à haute énergie peut être « diluée » sur l'ensemble du peptide ou de la protéine et provoque une fragmentation étendue du squelette peptidique (liaisons C-C), tandis que les photons IR à faible énergie augmentent progressivement l'énergie interne et dissocient préférentiellement les liaisons amide (C-N) les plus labiles.Cette thèse est centrée sur le développement de méthodes et les applications pour une caractérisation structurale de biomolécules par des méthodes d'activation utilisant des photons. L'intérêt de combiner des photons infrarouges à faible énergie et des photons UV à haute énergie dans un spectromètre de masse Orbitrap, pour la caractérisation de petites protéines, a été évalué. En outre, la dissociation infrarouge multiphotonique a été implémentée dans un piège à ions électrostatique afin d’étendre les méthodes de fragmentation aux macromolécules de très haut poids moléculaires dans le domaine mégadalton. L'une des principales avancées de cette thèse a été d'adapter ces méthodes de spectrométrie de masse aux objets biomoléculaires, allant des petits peptides (dans la gamme de masse de kilodalton) à des fibres de protéines entières (dans la gamme de masse de mégadalton) / The structural characterization of proteins often required them to be fragmented into small units containing only few amino acids. In bottom-up approach, proteins are cleaved into small peptides by enzyme then these peptides are subjected to further fragmentation in a collision cell of a tandem mass spectrometer. However, in top-down approach, proteins can directly be dissociated (without enzyme) into small fragments by collision, electron and photon-driven dissociations. Photon-based activation methods including ultraviolet photodissociation (UVPD) and infrared multiphoton dissociation (IRMPD) have received great attention as an alternative to electron-driven and collision induced dissociation methods. Absorption of the high-energy UV photon is dispersed over the whole peptide or protein and stimulates extensive C?Ca backbone fragmentation while the low-energy IR photons gradually increases the internal energy and thus favorably dissociates the most labile amide (C?N) bonds. This thesis focuses on the method development and applications for characterizing biomolecules by photon-based activation methods. The interest of combining high-energy UV photons and low-energy IR photons in an Orbitrap mass spectrometer, for protein and post-translationally modified peptide characterization, has been evaluated. Moreover, infrared multiphoton dissociation has been implemented in a gated electrostatic ion trap to push forward the limit of fragmentation methods to large megadalton ions. One of the main breakthroughs in this thesis is the ability to adapt these method developments and applications to biomolecular objects ranging from small peptides (in kilodalton mass range) to entire protein fibrils (in megadalton mass range)
|
Page generated in 0.1211 seconds