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Structural mass spectrometry strategies for systems biology

dc.creatorEnders, Jeffrey Richard
dc.date.accessioned2020-08-22T20:59:00Z
dc.date.available2014-12-17
dc.date.issued2012-12-17
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-09072012-084324
dc.identifier.urihttp://hdl.handle.net/1803/14097
dc.description.abstractSystems biology seeks to describe the function of a biological system using a holistic, multiscale approach. This approach encompasses the analyses of molecular classes such as the genome, transcriptome, proteome, and metabolome (among others) of a biological system. Systems biology asserts that while understanding genes and proteins is important, the most important aspects going forward are more closely related to the system’s network structure and network dynamics. There is a substantial need for improved techniques for coupling the system on which the analysis is being performed (i.e., the organism) with the detection instrumentation (i.e., the ion mobility-mass spectrometer). Advances in systems biology measurements which focus on improved dynamic detection strategies are presented in this work. Our preliminary research shows the potential for this system to provide temporally resolved systems biology data directly from complex cellular culture populations. Precise and expedient control of the microenvironment of the MTNP with regards to input concentrations (i.e., stimuli) has been demonstrated and shows that biomolecular temporal events on the order of 5 minutes are observable with this platform. This accomplishment is critical for future stimulus/response experiments. The broad and temporally accurate detection capabilities of IM-MS have been demonstrated for complex biological samples originating from a sustained yeast cellular culture inside of a microfluidic device. The potential of the combination of microfluidics and IM-MS has been shown by the sheer number of analytes detected from a simple Jurkat cell population. This Jurkat cell data illustrates the abundance of secreted material which is observable with the use of ion mobility-mass spectrometry. Additionally, we have reviewed a study on cocaine metabolism in Jurkat cells which benchmarks the platform while also demonstrating its potential for discovery-driven research.
dc.format.mimetypeapplication/pdf
dc.subjectMS
dc.subjectnetwork dynamics
dc.subjectcellular dynamics
dc.subjectsystems biology
dc.subjectmass spectrometry
dc.subjection mobility
dc.subjectmicrofluidics
dc.subjectsolid phase extraction
dc.subjectIM
dc.subjectSPE
dc.subjectonline SPE
dc.titleStructural mass spectrometry strategies for systems biology
dc.typedissertation
dc.contributor.committeeMemberDavid E. Cliffel
dc.contributor.committeeMemberBrian O. Bachmann
dc.contributor.committeeMemberJohn P. Wikswo
dc.type.materialtext
thesis.degree.namePHD
thesis.degree.leveldissertation
thesis.degree.disciplineChemistry
thesis.degree.grantorVanderbilt University
local.embargo.terms2014-12-17
local.embargo.lift2014-12-17
dc.contributor.committeeChairJohn A. McLean


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