Literature DB >> 18271578

Amyloid-beta(29-42) dimer formations studied by a multicanonical-multioverlap molecular dynamics simulation.

Satoru G Itoh1, Yuko Okamoto.   

Abstract

Amyloid-beta peptides are known to form amyloid fibrils and are considered to play an important role in Alzheimer's disease. Amyloid-beta(29-42) is a fragment of the amyloid-beta peptide and also has a tendency to form amyloid fibrils. In order to study the mechanism of amyloidogenesis of this fragment, we applied one of the generalized-ensemble algorithms, the multicanonical-multioverlap algorithm, to amyloid-beta(29-42) dimer in aqueous solution. We obtained a detailed free-energy landscape of the dimer system. From the detailed free-energy landscape, we examined monomer and dimer formations of amyloid-beta(29-42) and deduced dimerization processes, which correspond to seeding processes in the amyloidogenesis of amyloid-beta(29-42).

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Year:  2008        PMID: 18271578     DOI: 10.1021/jp712170h

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  16 in total

1.  Association thermodynamics and conformational stability of beta-sheet amyloid beta(17-42) oligomers: effects of E22Q (Dutch) mutation and charge neutralization.

Authors:  Nikolay Blinov; Lyudmyla Dorosh; David Wishart; Andriy Kovalenko
Journal:  Biophys J       Date:  2010-01-20       Impact factor: 4.033

2.  Simulating oligomerization at experimental concentrations and long timescales: A Markov state model approach.

Authors:  Nicholas W Kelley; V Vishal; Grant A Krafft; Vijay S Pande
Journal:  J Chem Phys       Date:  2008-12-07       Impact factor: 3.488

3.  Hydration effects on the HET-s prion and amyloid-beta fibrillous aggregates, studied with three-dimensional molecular theory of solvation.

Authors:  Takeshi Yamazaki; Nikolay Blinov; David Wishart; Andriy Kovalenko
Journal:  Biophys J       Date:  2008-08-08       Impact factor: 4.033

4.  Role of β-hairpin formation in aggregation: the self-assembly of the amyloid-β(25-35) peptide.

Authors:  Luca Larini; Joan-Emma Shea
Journal:  Biophys J       Date:  2012-08-08       Impact factor: 4.033

Review 5.  Insights into the Molecular Mechanisms of Alzheimer's and Parkinson's Diseases with Molecular Simulations: Understanding the Roles of Artificial and Pathological Missense Mutations in Intrinsically Disordered Proteins Related to Pathology.

Authors:  Orkid Coskuner-Weber; Vladimir N Uversky
Journal:  Int J Mol Sci       Date:  2018-01-24       Impact factor: 5.923

6.  Structures of beta-amyloid peptide 1-40, 1-42, and 1-55-the 672-726 fragment of APP-in a membrane environment with implications for interactions with gamma-secretase.

Authors:  Naoyuki Miyashita; John E Straub; D Thirumalai
Journal:  J Am Chem Soc       Date:  2009-12-16       Impact factor: 15.419

7.  Computational study of the binding of CuII to Alzheimer's amyloid-beta peptide: do Abeta42 and Abeta40 bind copper in identical fashion?

Authors:  Yogita Mantri; Marco Fioroni; Mu-Hyun Baik
Journal:  J Biol Inorg Chem       Date:  2008-07-08       Impact factor: 3.358

8.  All-atom computer simulations of amyloid fibrils disaggregation.

Authors:  Jun Wang; Chunhu Tan; Hai-Feng Chen; Ray Luo
Journal:  Biophys J       Date:  2008-08-29       Impact factor: 4.033

9.  Structural diversity of Alzheimer's disease amyloid-β dimers and their role in oligomerization and fibril formation.

Authors:  Igor F Tsigelny; Yuriy Sharikov; Valentina L Kouznetsova; Jerry P Greenberg; Wolfgang Wrasidlo; Tania Gonzalez; Paula Desplats; Sarah E Michael; Margarita Trejo-Morales; Cassia R Overk; Eliezer Masliah
Journal:  J Alzheimers Dis       Date:  2014       Impact factor: 4.472

10.  Unfolding of the amyloid β-peptide central helix: mechanistic insights from molecular dynamics simulations.

Authors:  Mika Ito; Jan Johansson; Roger Strömberg; Lennart Nilsson
Journal:  PLoS One       Date:  2011-03-07       Impact factor: 3.240

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