Glycoblotting method allows for rapid and efficient glycome profiling of human Alzheimer's disease brain, serum and cerebrospinal fluid towards potential biomarker discovery
| Autor: | Solomon T. Gizaw, Shin-Ichiro Nishimura, Hiroshi Hinou, Tetsu Ohashi, Masakazu Tanaka |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Male Glycosylation Biophysics Biology Biochemistry Glycosphingolipids Glycomics 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Cerebrospinal fluid Alzheimer Disease Polysaccharides medicine Humans Molecular Biology CSF albumin Glycoproteins Cerebral Cortex Human brain medicine.disease Glycome 030104 developmental biology medicine.anatomical_structure chemistry Immunology Biomarker (medicine) Female Alzheimer's disease 030217 neurology & neurosurgery Biomarkers |
| Zdroj: | Biochimica et biophysica acta. 1860(8) |
| ISSN: | 0006-3002 |
| Popis: | Background Understanding of the significance of posttranslational glycosylation in Alzheimer's disease (AD) is of growing importance for the investigation of the pathogenesis of AD as well as discovery research of the disease-specific serum biomarkers. Methods We designed a standard protocol for the glycoblotting combined with MALDI-TOFMS to perform rapid and quantitative profiling of the glycan parts of glycoproteins (N-glycans) and glycosphingolipids (GSLs) using human AD's post-mortem samples such as brain tissues (dissected cerebral cortices such as frontal, parietal, occipital, and temporal domains), serum and cerebrospinal fluid (CSF). Results The structural profiles of the major N-glycans released from glycoproteins and the total expression levels of the glycans were found to be mostly similar between the brain tissues of the AD patients and those of the normal control group. In contrast, the expression levels of the serum and CSF protein N-glycans such as bisect-type and multiply branched glycoforms were increased significantly in AD patient group. In addition, the levels of some gangliosides such as GM1, GM2 and GM3 appeared to alter in the AD patient brain and serum samples when compared with the normal control groups. Conclusion Alteration of the expression levels of major N- and GSL-glycans in human brain tissues, serum and CSF of AD patients can be monitored quantitatively by means of the glycoblotting-based standard protocols. General significance The changes in the expression levels of the glycans derived from the human post-mortem samples uncovered by the standardized glycoblotting method provides potential serum biomarkers in central nervous system disorders and can contribute to the insight into the molecular mechanisms in the pathogenesis of neurodegenerative diseases and future drug discovery. Most importantly, the present preliminary trials using human post-mortem samples of AD patients suggest that large-scale serum glycomics cohort by means of various-types of human AD patients as well as the normal control sera can facilitate the discovery research of highly sensitive and reliable serum biomarkers for an early diagnosis of AD. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. |
| Databáze: | OpenAIRE |
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