The amyloid-β (Aβ) peptide pattern in cerebrospinal fluid in Alzheimer's disease:: evidence of a novel carboxyterminally elongated Aβ peptide

被引:90
作者
Lewczuk, P
Esselmann, H
Meyer, M
Wollscheid, V
Neumann, M
Otto, M
Maler, JM
Rüther, E
Kornhuber, J
Wiltfang, J
机构
[1] Univ Erlangen Nurnberg, Mol Neurobiol Lab, Dept Psychiat & Psychotherapy, D-91054 Erlangen, Germany
[2] Univ Gottingen, Dept Psychiat, D-37075 Gottingen, Germany
[3] Ciphergen Biosyst GmbH, D-37085 Gottingen, Germany
[4] Univ Munich, Inst Neuropathol, D-81377 Munich, Germany
[5] Univ Gottingen, Dept Neurol, D-37075 Gottingen, Germany
关键词
D O I
10.1002/rcm.1048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The patterns of amyloid beta (Abeta) peptides in human cerebrospinal fluid (CSF) and brain homogenates were studied by surface-enhanced laser desorption/ionization (SELDI) time-of-flight (TOF) mass spectrometry, and the results were compared with those obtained by Abeta-SDS-PAGE/immunoblot. Apart from the peptides known in the literature to occur in the CSF, we postulate the existence of a novel, previously not described peptide, either Abeta1-45 or Abeta2-46. This peptide was observed exclusively in a pool of samples originating from patients with AD, i.e. CSF and postmortem brain homogenates, but not in either the pooled CSF samples nor the pooled brain homogenates of the non-demented controls. Similarly to our previous results, Abeta1-42 was decreased in the CSF in AD. Expectedly, brain homogenates of the control subjects did not show the presence of Abeta peptides. Compared with Abeta-SDS-PAGE/immunoblot, SELDI-TOF enabled more precise analysis of Abeta peptides in the human material. We conclude that SELDI-TOF offers a promising tool for dementia expression pattern profiling using a minute amount of a biological sample. Copyright (C) 2003 John Wiley Sons, Ltd.
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收藏
页码:1291 / 1296
页数:6
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