Abstract
Glycoproteins in cerebrospinal fluid (CSF) are altered in Alzheimer's Disease (AD) patients compared to control individuals. We have utilized albumin depletion prior to 2D gel electrophoresis to enhance glycoprotein concentration for image analysis as well as structural glycoprotein determination without glycan release using mass spectrometry (MS). The benefits of a direct glycoprotein analysis approach include minimal sample manipulation and retention of structural details. A quantitative comparison of gel-separated glycoprotein isoforms from twelve AD patients and twelve control subjects was performed with glycoprotein-specific and total protein stains. We have also compared glycoforms in pooled CSF obtained from AD patients and control subjects with mass spectrometry. One isoform of α1-antitrypsin showed decreased glycosylation in AD patients while another glycosylated isoform of an unassigned protein was up-regulated. Protein expression levels of α1- antitrypsin were decreased, while the protein levels of apolipoprotein E and clusterin were increased in AD. No specific glycoform could be specifically assigned to AD.
Original language | English (US) |
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Pages (from-to) | 1332-1340 |
Number of pages | 9 |
Journal | Neurochemical Research |
Volume | 33 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2008 |
Externally published | Yes |
Keywords
- Alzheimer's Disease
- Apolipoprotein E
- CSF
- Cerebrospinal fluid
- Clusterin
- Glycoform
- Glycoprotein
- Glycoproteomics
- Glycosylation
- Haptoglobin
- Isoform
- N-linked
- Proteomics
- α- antitrypsin
- α-1-β-glycoprotein
ASJC Scopus subject areas
- Biochemistry
- Cellular and Molecular Neuroscience