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Glycoproteomics in neurodegenerative diseases

dc.contributor.authorHwang, Hyejinen_US
dc.contributor.authorZhang, Jianpengen_US
dc.contributor.authorChung, Kathryn A.en_US
dc.contributor.authorLeverenz, James B.en_US
dc.contributor.authorZabetian, Cyrus P.en_US
dc.contributor.authorPeskind, Elaine R.en_US
dc.contributor.authorJankovic, Josephen_US
dc.contributor.authorSu, Zhenen_US
dc.contributor.authorHancock, Aneeka M.en_US
dc.contributor.authorPan, Catherineen_US
dc.contributor.authorMontine, Thomas J.en_US
dc.contributor.authorPan, Shengen_US
dc.contributor.authorNutt, Johnen_US
dc.contributor.authorAlbin, Roger L.en_US
dc.contributor.authorGearing, Marlaen_US
dc.contributor.authorBeyer, Richard P.en_US
dc.contributor.authorShi, Minen_US
dc.contributor.authorZhang, Jingen_US
dc.date.accessioned2010-01-05T15:08:45Z
dc.date.available2011-03-01T16:26:44Zen_US
dc.date.issued2010-01en_US
dc.identifier.citationHwang, Hyejin; Zhang, Jianpeng; Chung, Kathryn A.; Leverenz, James B.; Zabetian, Cyrus P.; Peskind, Elaine R.; Jankovic, Joseph; Su, Zhen; Hancock, Aneeka M.; Pan, Catherine; Montine, Thomas J.; Pan, Sheng; Nutt, John; Albin, Roger; Gearing, Marla; Beyer, Richard P.; Shi, Min; Zhang, Jing (2010). "Glycoproteomics in neurodegenerative diseases." Mass Spectrometry Reviews 29(1): 79-125. <http://hdl.handle.net/2027.42/64521>en_US
dc.identifier.issn0277-7037en_US
dc.identifier.issn1098-2787en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/64521
dc.description.abstractProtein glycosylation regulates protein function and cellular distribution. Additionally, aberrant protein glycosylations have been recognized to play major roles in human disorders, including neurodegenerative diseases. Glycoproteomics, a branch of proteomics that catalogs and quantifies glycoproteins, provides a powerful means to systematically profile the glycopeptides or glycoproteins of a complex mixture that are highly enriched in body fluids, and therefore, carry great potential to be diagnostic and/or prognostic markers. Application of this mass spectrometry-based technology to the study of neurodegenerative disorders (e.g., Alzheimer's disease and Parkinson's disease) is relatively new, and is expected to provide insight into the biochemical pathogenesis of neurodegeneration, as well as biomarker discovery. In this review, we have summarized the current understanding of glycoproteins in biology and neurodegenerative disease, and have discussed existing proteomic technologies that are utilized to characterize glycoproteins. Some of the ongoing studies, where glycoproteins isolated from cerebrospinal fluid and human brain are being characterized in Parkinson's disease at different stages versus controls, are presented, along with future applications of targeted validation of brain specific glycoproteins in body fluids. © 2009 Wiley Periodicals, Inc., Mass Spec Rev 29:79–125, 2010en_US
dc.format.extent2156410 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherAnalytical Chemistry and Spectroscopyen_US
dc.titleGlycoproteomics in neurodegenerative diseasesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumAnn Arbor VAMC GRECC and Department of Neurology, University of Michigan, Ann Arbor, MIen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Neurology, Oregon Health and Science University, Portland, ORen_US
dc.contributor.affiliationotherDepartment of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA ; Department of Neurology, University of Washington School of Medicine, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Neurology, University of Washington School of Medicine, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA ; Department of Neurology, University of Washington School of Medicine, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Neurology, Baylor College of Medicine, Houston, TXen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Neurology, Oregon Health and Science University, Portland, ORen_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, GAen_US
dc.contributor.affiliationotherDepartment of Environmental & Occupational Health Sciences, University of Washington School of Medicine, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Washington, Seattle, WA ; Department of Pathology, University of Washington School of Medicine, HMC Box 359635, Seattle, WA 98104.en_US
dc.identifier.pmid19358229en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/64521/1/20221_ftp.pdf
dc.identifier.doi10.1002/mas.20221en_US
dc.identifier.sourceMass Spectrometry Reviewsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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