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dc.contributor.advisorChairperson, Graduate Committee: Paul Grieco; Hien Hguyen (co-chair)en
dc.contributor.authorSpicka, Kevin Jamesen
dc.description.abstractProteomics is a rapidly developing field requiring powerful new technology in order to be able to detect proteins at increasingly lower concentrations. To aid in the detection of proteins at lower concentrations, DIGE dyes, a family of spectrally resolved fluorescent dyes, are currently available to proteomic researchers for 2D gel analysis. However, the demands of protein detection dictate that dyes that are even more sensitive and versatile be created. The syntheses of highly sensitive, water soluble BODIPY fluorophore dyes are described. These dyes are proposed to have the necessary sensitivity to allow for detection of proteins in much lower concentrations, providing an improvement over current protein detection limits. The BODIPY dyes that have been synthesized are available in a variety of absorbances and emissions. While fluorescent dyes that are amine-reactive are the most popular covalently binding protein labeling markers being used in today's proteomic research, thiol-reactive fluorescent markers are gaining importance in proteomic research. Since thiol residues are less common in proteins compared to their amine counterparts, saturation labeling and quantification are more easily achieved. The syntheses of sensitive thiol- reactive fluorescent dyes are described. These syntheses allow for quick generation of thiol-reactive fluorescent markers to be used in proteomic research.en
dc.publisherMontana State University - Bozeman, College of Letters & Scienceen
dc.subject.lcshFluorescence spectroscopy.en
dc.titleDesign and synthesis of fluorescent dyes for use in proteomic researchen
dc.rights.holderCopyright 2008 by Kevin James Spickaen
thesis.catalog.ckey1457739en, Graduate Committee: Edward Dratz; Thomas S. Livinghouse; Mary J. Cloningeren & Biochemistry.en

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