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      Stability of single and double layer fibrillar amyloid-β oligomers

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      1 , 1 , 1 ,
      Journal of Cheminformatics
      BioMed Central
      8th German Conference on Chemoinformatics: 26 CIC-Workshop
      11-13 November 2012

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          Abstract

          Alzheimer's disease (AD) is the most common form of dementia world-wide. The causative agent in this protein misfolding disease is the 39 to 42-residues long amyloid-β (Aβ) peptide, that aggregates into oligomers, filaments, and fibrils found in plaque deposits in the brain of AD patients [1]. Up to now a viable cure for this disease is still not available. One reason for this is Aβ's conformational flexibility and structural heterogeneity in solution paired with its aggregation tendency. This renders the determination and isolation of distinct Aβ structures experimentally challenging. Especially the soluble oligomers, that are thought to be the neurotoxic species in AD, may adopt a plethora of conformations in vivo [1]. It is known from experiment, that there exist toxic fibrillar oligomers, but the details of their topology are not yet known [2]. Thus, we used molecular dynamics simulations to investigate the structural stability of fibrillar single and ouble layer Aβ42 oligomers of different size (4-mer to 48-mer), that we constructed from the experimental structure [3] (cf Figure 1). Figure 1 Double layer Aβ 48-mer (Met35 in the interface in sticks representation). We found that there is a clear correlation between oligomer size and preference for double layer structure: Large oligomers display an enhanced stability in double layer conformation, whereas small oligomers prefer the single layer structure. On the other hand, large single layer oligomers dissociate into smaller oligomers, while small double layer oligomers collapse or are energetically unfavorable. From our simulations we deduce that the critical number of oligomers to construct a stable Aβ double layer is in the range of 10 to 12. In a more general picture, longitudinal growth along a single layer is limited by the increasing structural instability. Lateral growth, i.e. forming a double layer, creates stable mini-fibrils. These may act as seeds for further stable fibril growth.

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          Toxic fibrillar oligomers of amyloid-β have cross-β structure.

          Although amyloid fibers are found in neurodegenerative diseases, evidence points to soluble oligomers of amyloid-forming proteins as the cytotoxic species. Here, we establish that our preparation of toxic amyloid-β(1-42) (Abeta42) fibrillar oligomers (TABFOs) shares with mature amyloid fibrils the cross-β structure, in which adjacent β-sheets adhere by interpenetration of protein side chains. We study the structure and properties of TABFOs by powder X-ray diffraction, EM, circular dichroism, FTIR spectroscopy, chromatography, conformational antibodies, and celluar toxicity. In TABFOs, Abeta42 molecules stack into short protofilaments consisting of pairs of helical β-sheets that wrap around each other to form a superhelix. Wrapping results in a hole along the superhelix axis, providing insight into how Abeta may form pathogenic amyloid pores. Our model is consistent with numerous properties of Abeta42 fibrillar oligomers, including heterogenous size, ability to seed new populations of fibrillar oligomers, and fiber-like morphology.
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            Author and article information

            Conference
            J Cheminform
            J Cheminform
            Journal of Cheminformatics
            BioMed Central
            1758-2946
            2013
            22 March 2013
            : 5
            : Suppl 1
            : P9
            Affiliations
            [1 ]Bioinformatik, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany
            Article
            1758-2946-5-S1-P9
            10.1186/1758-2946-5-S1-P9
            3606172
            f5e1fc0f-13d6-4a8a-8005-f245b8ebee42
            Copyright ©2013 Kahler et al.; licensee BioMed Central Ltd.

            This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

            8th German Conference on Chemoinformatics: 26 CIC-Workshop
            Goslar, Germany
            11-13 November 2012
            History
            Categories
            Poster Presentation

            Chemoinformatics
            Chemoinformatics

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