Sensitive detection of Aβ protofibrils by proximity ligation - relevance for Alzheimer's disease

被引:31
作者
Kamali-Moghaddam, Masood [1 ]
Pettersson, Frida Ekholm [2 ]
Wu, Di [1 ]
Englund, Hillevi [2 ]
Darmanis, Spyros [1 ]
Lord, Anna [2 ]
Tavoosidana, Gholamreza [1 ]
Sehlin, Dag [2 ]
Gustafsdottir, Sigrun [1 ]
Nilsson, Lars N. G. [2 ]
Lannfelt, Lars [2 ]
Landegren, Ulf [1 ]
机构
[1] Uppsala Univ, Dept Genet & Pathol, Uppsala, Sweden
[2] Uppsala Univ, Dept Publ Hlth & Caring Sci, Uppsala, Sweden
来源
BMC NEUROSCIENCE | 2010年 / 11卷
基金
瑞典研究理事会;
关键词
POTENTIATION IN-VIVO; TRANSGENIC MICE; NEUROTOXICITY; OLIGOMERS; ASSAYS; FLUID;
D O I
10.1186/1471-2202-11-124
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Protein aggregation plays important roles in several neurodegenerative disorders. For instance, insoluble aggregates of phosphorylated tau and of A beta peptides are cornerstones in the pathology of Alzheimer's disease. Soluble protein aggregates are therefore potential diagnostic and prognostic biomarkers for their cognate disorders. Detection of the aggregated species requires sensitive tools that efficiently discriminate them from monomers of the same proteins. Here we have established a proximity ligation assay (PLA) for specific and sensitive detection of A beta protofibrils via simultaneous recognition of three identical determinants present in the aggregates. PLA is a versatile technology in which the requirement for multiple target recognitions is combined with the ability to translate signals from detected target molecules to amplifiable DNA strands, providing very high specificity and sensitivity. Results: For specific detection of A beta protofibrils we have used a monoclonal antibody, mAb158, selective for A beta protofibrils in a modified PLA, where the same monoclonal antibody was used for the three classes of affinity reagents required in the assay. These reagents were used for detection of soluble Ab aggregates in solid- phase reactions, allowing detection of just 0.1 pg/ml A beta protofibrils, and with a dynamic range greater than six orders of magnitude. Compared to a sandwich ELISA setup of the same antibody the PLA increases the sensitivity of the Ab protofibril detection by up to 25- fold. The assay was used to measure soluble Ab aggregates in brain homogenates from mice transgenic for a human allele predisposing to A beta aggregation. Conclusions: The proximity ligation assay is a versatile analytical technology for proteins, which can provide highly sensitive and specific detection of A beta aggregates - and by implication other protein aggregates of relevance in Alzheimer's disease and other neurodegenerative disorders.
引用
收藏
页数:7
相关论文
共 21 条
  • [1] Sensitive Plasma Protein Analysis by Microparticle-based Proximity Ligation Assays
    Darmanis, Spyros
    Nong, Rachel Yuan
    Hammond, Maria
    Gu, Jijuan
    Alderborn, Anders
    Vanelid, Johan
    Siegbahn, Agneta
    Gustafsdottir, Sigrun
    Ericsson, Olle
    Landegren, Ulf
    Kamali-Moghaddam, Masood
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (02) : 327 - 335
  • [2] Sensitive ELISA detection of amyloid-β protofibrils in biological samples
    Englund, Hillevi
    Sehlin, Dag
    Johansson, Ann-Sofi
    Nilsson, Lars N. G.
    Gellerfors, Paer
    Paulie, Staffan
    Lannfelt, Lars
    Pettersson, Frida Ekholm
    [J]. JOURNAL OF NEUROCHEMISTRY, 2007, 103 (01) : 334 - 345
  • [3] Oligomerization Partially Explains the Lowering of Aβ42 in Alzheimer's Disease Cerebrospinal Fluid
    Englund, Hillevi
    Gunnarsson, Malin Degerman
    Brundin, Rose Marie
    Hedlund, Marie
    Kilander, Lena
    Lannfelt, Lars
    Pettersson, Frida Ekholm
    [J]. NEURODEGENERATIVE DISEASES, 2009, 6 (04) : 139 - 147
  • [4] Protein detection using proximity-dependent DNA ligation assays
    Fredriksson, S
    Gullberg, M
    Jarvius, J
    Olsson, C
    Pietras, K
    Gústafsdóttir, SM
    Östman, A
    Landegren, U
    [J]. NATURE BIOTECHNOLOGY, 2002, 20 (05) : 473 - 477
  • [5] FUKUMOTO H, FASEB J, V24, P2716
  • [6] Nanoparticle-based detection in cerebral spinal fluid of a soluble pathogenic biomarker for Alzheimer's disease
    Georganopoulou, DG
    Chang, L
    Nam, JM
    Thaxton, CS
    Mufson, EJ
    Klein, WL
    Mirkin, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (07) : 2273 - 2276
  • [7] Cytokine detection by antibody-based proximity ligation
    Gullberg, M
    Gústafsdóttir, SM
    Schallmeiner, E
    Jarvius, J
    Bjarnegård, M
    Betsholtz, C
    Landegren, U
    Fredriksson, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (22) : 8420 - 8424
  • [8] Detection of individual microbial pathogens by proximity ligation
    Gustafsdottir, Sigrun M.
    Nordengrahn, Ann
    Fredriksson, Simon
    Wallgren, Per
    Rivera, Esteban
    Schallmeiner, Edith
    Merza, Malik
    Landegren, Ulf
    [J]. CLINICAL CHEMISTRY, 2006, 52 (06) : 1152 - 1160
  • [9] Association between CSF biomarkers and incipient Alzheimer's disease in patients with mild cognitive impairment: a follow-up study
    Hansson, O
    Zetterberg, H
    Buchhave, P
    Londos, E
    Blennow, K
    Minthon, L
    [J]. LANCET NEUROLOGY, 2006, 5 (03) : 228 - 234
  • [10] Protofibrillar intermediates of amyloid β-protein induce acute electrophysiological changes and progressive neurotoxicity in cortical neurons
    Hartley, DM
    Walsh, DM
    Ye, CPP
    Diehl, T
    Vasquez, S
    Vassilev, PM
    Teplow, DB
    Selkoe, DJ
    [J]. JOURNAL OF NEUROSCIENCE, 1999, 19 (20) : 8876 - 8884