Differently Selected D-Enantiomeric Peptides Act on Different Aβ Species

被引:21
作者
Bartnik, Dirk [2 ]
Funke, Susanne Aileen [1 ]
Andrei-Selmer, Luminita-Cornelia [3 ]
Bacher, Michael [3 ]
Dodel, Richard [3 ]
Willbold, Dieter [1 ,2 ]
机构
[1] Forschungszentrum Julich, ISB 3, D-52425 Julich, Germany
[2] Univ Dusseldorf, Inst Phys Biol, D-40225 Dusseldorf, Germany
[3] Univ Marburg, Dept Neurol, Biomed Forschungszentrum, D-35037 Marburg, Germany
关键词
IMAGE PHAGE DISPLAY; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; PROTEIN OLIGOMERS;
D O I
10.1089/rej.2009.0924
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Aging is the most significant risk factor for Alzheimer disease (AD). The pathological hallmark of AD is the accumulation of aggregated amyloid-beta (A beta) forms and insoluble plaques, mainly composed of A beta, in the brain of the patient. Recently, we reported on the selection of D-enantiomeric, A beta-binding peptides D1 and D3. D1 was selected against aggregated A beta species to address diagnosis by in vivo imaging of amyloid plaques, whereas D3 was selected using low-molecular-weight A beta species, therefore addressing therapeutical studies. Here, we use a surface plasmon resonance method to confirm that both peptides show the desired binding specificities.
引用
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页码:202 / 205
页数:4
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