Development of Aβ terminal end-specific antibodies and sensitive ELISA for Aβ variant

被引:76
作者
Horikoshi, Y
Sakaguchi, G
Becker, AG
Gray, AJ
Duff, K
Aisen, PS
Yamaguchi, H
Maeda, M
Kinoshita, N
Matsuoka, Y [1 ]
机构
[1] NYU, Sch Med, Nathan S Kline Inst Psychiat Res, Ctr Dementia Res, Orangeburg, NY 10962 USA
[2] Immunobiol Labs Co Ltd, Fujioka, Gunma 375005, Japan
[3] Gunma Univ, Sch Hlth Sci, Maebashi, Gumma 3718514, Japan
[4] Georgetown Univ, Med Ctr, Dept Neurol, Washington, DC 20057 USA
基金
美国国家卫生研究院;
关键词
Alzheimer; dementia; amyloid; A beta; antibody; beta-secretase; ELISA; histochemistry; western;
D O I
10.1016/j.bbrc.2004.05.051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative affliction associated with memory dysfunction. Senile plaques are a pathological hallmark of AD, and amyloid beta (Abeta) peptides are a major component of these plaques. Abeta peptides are derived from proteolytic cleavage of the Abeta protein precursor (APP) by beta- and gamma-secretases to generate two principal species, Abeta1-40 and Abeta1-42. We have developed antibodies against the N- and C-termini of these peptides, and an ELISA for accurate and sensitive quantitative assessment. Sandwich ELISA composed of N-terminus (Abeta1) end-specific antibody, clone 82E1, and C-termini end-specific antibodies, and clones 1A10 and IC3 for Abeta40 and Abeta42, respectively, detects full-length Abeta1-40 and 1-42 with a sensitivity in the sub single digit fmol/ml (equivalent to single digit pg/ml) range with no cross-reactivity to APP. A combination of C-termini antibodies and an antibody against the middle region of Abeta detects mouse Abeta in non-transgenic mouse brains. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:733 / 737
页数:5
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