In-situ atomic force microscopy study of β-amyloid fibrillization

被引:154
作者
Blackley, HKL
Sanders, GHW
Davies, MC
Roberts, CJ
Tendler, SJB
Wilkinson, MJ
机构
[1] Univ Nottingham, Sch Pharmaceut Sci, Lab Biophys & Surface Anal, Nottingham NG7 2RD, England
[2] SmithKline Beecham Pharmaceut, Microscopy Analyt Sci, NFSP, Harlow CM19 5AW, Essex, England
基金
英国生物技术与生命科学研究理事会;
关键词
beta-amyloid; Alzheimer's disease; atomic force microscopy; fibril formation; protofibril;
D O I
10.1006/jmbi.2000.3711
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
We report the use of atomic force microscopy to observe the initial stages of beta-amyloid fibrillization in situ. The growth of individual beta-amyloid protofibrils on a mica substrate was followed over several hours. The first in situ visualization of protofibril formation from single aggregate units of beta-amyloid is reported. The growth of these protofibrils through the subsequent addition of these aggregate units is also observed. Growth of the protofibrils is bi-directional and the outgrowth of protofibrils from a common amyloid/heterogeneous core is also observed. Elongation also occurred by the addition of protofibrils from solution. This data provides an exciting insight into the early stages of beta-amyloid fibrillization and can be used to enhance the understanding of the mechanism(s) by which beta-amyloid fibrillizes and may consequently enable inhibition of one or more stages of fibrillization as a potential therapeutic strategy. (C) 2000 Academic Press.
引用
收藏
页码:833 / 840
页数:8
相关论文
共 27 条
[1]   Morphological development of β(1-40) amyloid fibrils [J].
Blackley, HKL ;
Patel, N ;
Davies, MC ;
Roberts, CJ ;
Tendler, SJB ;
Wilkinson, MJ ;
Williams, PM .
EXPERIMENTAL NEUROLOGY, 1999, 158 (02) :437-443
[2]   GENERATION OF BETA-AMYLOID IN THE SECRETORY PATHWAY IN NEURONAL AND NONNEURONAL CELLS [J].
BUSCIGLIO, J ;
GABUZDA, DH ;
MATSUDAIRA, P ;
YANKNER, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :2092-2096
[3]   In vitro growth of Alzheimer's disease beta-amyloid plaques displays first-order kinetics [J].
Esler, WP ;
Stimson, ER ;
Ghilardi, JR ;
Vinters, HV ;
Lee, JP ;
Mantyh, PW ;
Maggio, JE .
BIOCHEMISTRY, 1996, 35 (03) :749-757
[4]   ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN [J].
GLENNER, GG ;
WONG, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (03) :885-890
[5]   Watching amyloid fibrils grow by time-lapse atomic force microscopy [J].
Goldsbury, C ;
Kistler, J ;
Aebi, U ;
Arvinte, T ;
Cooper, GJS .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 285 (01) :33-39
[6]   AMYLOID BETA-PEPTIDE IS PRODUCED BY CULTURED-CELLS DURING NORMAL METABOLISM [J].
HAASS, C ;
SCHLOSSMACHER, MG ;
HUNG, AY ;
VIGOPELFREY, C ;
MELLON, A ;
OSTASZEWSKI, BL ;
LIEBERBURG, I ;
KOO, EH ;
SCHENK, D ;
TEPLOW, DB ;
SELKOE, DJ .
NATURE, 1992, 359 (6393) :322-325
[7]   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
[8]   Atomic force microscopic imaging of seeded fibril formation and fibril branching by the Alzheimer's disease amyloid-β protein [J].
Harper, JD ;
Lieber, CM ;
Lansbury, PT .
CHEMISTRY & BIOLOGY, 1997, 4 (12) :951-959
[9]   Observation of metastable A beta amyloid protofibrils by atomic force microscopy [J].
Harper, JD ;
Wong, SS ;
Lieber, CM ;
Lansbury, PT .
CHEMISTRY & BIOLOGY, 1997, 4 (02) :119-125
[10]   AGGREGATION STATE AND NEUROTOXIC PROPERTIES OF ALZHEIMER BETA-AMYLOID PEPTIDE [J].
HOWLETT, DR ;
JENNINGS, KH ;
LEE, DC ;
CLARK, MSG ;
BROWN, F ;
WETZEL, R ;
WOOD, SJ ;
CAMILLERI, P ;
ROBERTS, GW .
NEURODEGENERATION, 1995, 4 (01) :23-32