Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7148
Title: Specific reactivity of mild/severe Alzheimer's disease patient's sera to antibody against Aß1-40 epitope 17-21
Authors: Bölükbaşı Hatip, Funda Fatma
Matsunaga, Y.
Yamada, T.
Keywords: Aß1-40
Dot blot
ELISA
Monoclonal antibody 4G8 temperature
Proteinase K
Severe and mild Alzheimer's disease
amyloid beta protein[1-40]
epitope
monoclonal antibody
proteinase K
adult
aged
Alzheimer disease
antibody specificity
article
clinical article
controlled study
disease severity
dot hybridization
enzyme linked immunosorbent assay
epitope mapping
female
gene sequence
human
immunoreactivity
male
protein aggregation
protein structure
serum
temperature dependence
Aged
Aged, 80 and over
Alzheimer Disease
Amyloid beta-Protein
Antibodies, Monoclonal
Endopeptidase K
Epitopes
Female
Humans
Immune Sera
Male
Middle Aged
Peptide Fragments
Abstract: Objectives - To detect the reactivity pattern of sera from patients with mild and severe Alzheimer's disease (AD) to specific antibodies targeting different epitopes in the primary structure of amyloid-beta (Aß). Materials and methods - Sera from patients diagnosed with mild or severe AD were used. The reactivity of sera to monoclonal antibodies recognizing 1-7, 5-10, 9-14 and 17-21 epitopes of Aß1-40 at 36-42°C was determined by an enzyme-linked immunosorbent assay. Proteinase K digestion of Aß1-40 was investigated by dot blotting at 36 and 40°C. Results: - Sera of patients with AD displayed reactivity only with monoclonal antibody recognizing the epitope 17-21 (4G8). The reactivity of sera from patients with severe AD was less than that of sera from patients with mild AD at temperatures 36-41°C, with no difference at 42°C. Patients with severe AD displayed lesser digestion with proteinase K. Conclusions - Sera derived from patients with AD could react with monoclonal antibodies directed to 17-21 sequences of Aß1-40 in a temperature-dependent manner. The severity of AD is associated with greater Aß1-40 aggregation and resistance to proteinase K. The present results may be of value in staging and following up of patients with AD. Copyright © 2007 The Authors.
URI: https://hdl.handle.net/11499/7148
https://doi.org/10.1111/j.1600-0404.2007.00959.x
ISSN: 0001-6314
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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