Oligomerization and toxicity of β-amyloid-42 implicated in Alzheimer's disease

被引:180
作者
El-Agnaf, OMA [1 ]
Mahil, DS [1 ]
Patel, BP [1 ]
Austen, BM [1 ]
机构
[1] Univ London St Georges Hosp, Sch Med, Dept Surg, Neurodegenerat Unit, London SW17 0RE, England
关键词
amyloid; Alzheimer's disease; oligomerization; solid-phase peptide synthesis; aggregation; toxicity;
D O I
10.1006/bbrc.2000.3051
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
beta-Amyloid protein (A beta) is the major component of senile plaques found in the brains of Alzheimer's patients. A novel ELISA has been developed which probes the early stages of oligomerization of A beta. Incubation of A beta solutions at 37 degrees C and pH 7.4 produces soluble oligomers in a concentration-dependent manner. Fresh A beta 42 solutions rapidly form soluble oligomers, whereas A beta 40 solutions require prolonged incubation to produce oligomers. Fresh A beta 42 solutions are more toxic to human neuroblastoma SH-SY5Y cells than A beta 40 solutions, possibly mediated by soluble oligomers. The differences between A beta 42 and A beta 40 could explain the association of the longer form with familial early-onset Alzheimer's disease. We also report a new strategy for solid-phase synthesis of A beta peptides which gives high yield and purity of the initial crude preparation. (C) 2000 Academic Press.
引用
收藏
页码:1003 / 1007
页数:5
相关论文
共 23 条
[1]  
Clements A, 1996, J NEUROCHEM, V66, P740
[2]   Synthesis and secondary structural studies of penta(acetyl-Hmb)Aβ(1-40) [J].
Clippingdale, AB ;
Macris, M ;
Wade, JD ;
Barrow, CJ .
JOURNAL OF PEPTIDE RESEARCH, 1999, 53 (06) :665-672
[3]   Acceleration of oligomerization, not fibrillization, is a shared property of both α-synuclein mutations linked to early-onset Parkinson's disease:: Implications for pathogenesis and therapy [J].
Conway, KA ;
Lee, SJ ;
Rochet, JC ;
Ding, TT ;
Williamson, RE ;
Lansbury, PT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (02) :571-576
[4]   The influence of the central region containing residues 19-25 on the aggregation properties and secondary structure of Alzheimer's β-amyloid peptide [J].
El-Agnaf, OMA ;
Guthrie, DJS ;
Walsh, DM ;
Irvine, GB .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 256 (03) :560-569
[5]  
El-Agnaf OMA, 2000, PROTEIN PEPTIDE LETT, V7, P1
[6]   Aggregates from mutant and wild-type α-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of β-sheet and amyloid-like filaments [J].
El-Agnaf, OMA ;
Jakes, R ;
Curran, MD ;
Middleton, D ;
Ingenito, R ;
Bianchi, E ;
Pessi, A ;
Neill, D ;
Wallace, A .
FEBS LETTERS, 1998, 440 (1-2) :71-75
[7]  
El-Agnaf Omar M. A., 1994, Letters in Peptide Science, V1, P135, DOI 10.1007/BF00128531
[8]   Assembly of Aβ amyloid protofibrils:: An in vitro model for a possible early event in Alzheimer's disease [J].
Harper, JD ;
Wong, SS ;
Lieber, CM ;
Lansbury, PT .
BIOCHEMISTRY, 1999, 38 (28) :8972-8980
[9]   Protofibrillar intermediates of amyloid β-protein induce acute electrophysiological changes and progressive neurotoxicity in cortical neurons [J].
Hartley, DM ;
Walsh, DM ;
Ye, CPP ;
Diehl, T ;
Vasquez, S ;
Vassilev, PM ;
Teplow, DB ;
Selkoe, DJ .
JOURNAL OF NEUROSCIENCE, 1999, 19 (20) :8876-8884
[10]   THE CARBOXY TERMINUS OF THE BETA-AMYLOID PROTEIN IS CRITICAL FOR THE SEEDING OF AMYLOID FORMATION - IMPLICATIONS FOR THE PATHOGENESIS OF ALZHEIMERS-DISEASE [J].
JARRETT, JT ;
BERGER, EP ;
LANSBURY, PT .
BIOCHEMISTRY, 1993, 32 (18) :4693-4697