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Protein Changes in Immunodepleted Cerebrospinal Fluid from a Transgenic Mouse Model of Alexander Disease Detected Using Mass Spectrometry

By Robert Cunningham (1998031), Paige Jany (1998028), Albee Messing (320554) and Lingjun Li (548329)


Cerebrospinal fluid (CSF) is a low protein content biological fluid with a dynamic range spanning at least 9 orders of magnitude in protein content and is in direct contact with the brain. A modified IgY-14 immunodepletion treatment was performed to enhance analysis of the low volumes of CSF that are obtainable from mice. As a model system in which to test this approach, we utilized transgenic mice that overexpress the intermediate filament glial fibrillary acidic protein (GFAP). These mice are models for Alexander disease (AxD), a severe leukodystrophy in humans. From the CSF of control and transgenic mice we report the identification of 289 proteins, with relative quantification of 103 proteins. Biological and technical triplicates were performed to address animal variability as well as reproducibility in mass spectrometric analysis. Relative quantitation was performed using distributive normalized spectral abundance factor (dNSAF) spectral counting analysis. A panel of biomarker proteins with significant changes in the CSF of GFAP transgenic mice has been identified with validation from enzyme-linked immunosorbent assay (ELISA) and microarray data, demonstrating the utility of our methodology and providing interesting targets for future investigations on the molecular and pathological aspects of AxD

Topics: Biochemistry, Cell Biology, Genetics, Molecular Biology, Neuroscience, Physiology, Biotechnology, Immunology, Chemical Sciences not elsewhere classified, Immunodepleted Cerebrospinal Fluid, CSF, Alexander Disease Detected, ELISA, Mass SpectrometryCerebrospinal fluid, protein content, address animal variability, filament glial fibrillary acidic protein, GFAP, Transgenic Mouse Model, analysis
Year: 2013
DOI identifier: 10.1021/pr300785h.s001
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Provided by: FigShare
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