Literature DB >> 30821034

A DFT-Assisted Topological Analysis of Four Polymorphic, S-Shaped Aβ42 Fibril Structures.

Alejandro R Foley1, Jevgenij A Raskatov1.   

Abstract

Amyloid β 42 (Aβ42) is an inherently disordered peptide, whose toxic actions are believed to play important roles in the etiology of Alzheimer's disease. Four fibril structures of the peptide that display broadly similar characteristics were recently published, but a systematic comparison of these structures is lacking. In this paper, a topological framework was created to enable such understanding and produced new insights into subtle structural elements that underlie the overall structural diversity. A DFT-based analysis illuminated some of the energetic differences that arise as a consequence.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amyloid beta-peptides; foldamers; hydrophobic interactions; topology

Mesh:

Substances:

Year:  2019        PMID: 30821034      PMCID: PMC6713286          DOI: 10.1002/cbic.201900036

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  19 in total

1.  In silico study of amyloid beta-protein folding and oligomerization.

Authors:  B Urbanc; L Cruz; S Yun; S V Buldyrev; G Bitan; D B Teplow; H E Stanley
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-06       Impact factor: 11.205

Review 2.  Protein misfolding, functional amyloid, and human disease.

Authors:  Fabrizio Chiti; Christopher M Dobson
Journal:  Annu Rev Biochem       Date:  2006       Impact factor: 23.643

3.  The Alzheimer's peptides Abeta40 and 42 adopt distinct conformations in water: a combined MD / NMR study.

Authors:  Nikolaos G Sgourakis; Yilin Yan; Scott A McCallum; Chunyu Wang; Angel E Garcia
Journal:  J Mol Biol       Date:  2007-03-07       Impact factor: 5.469

4.  Iridium-catalyzed allylic substitutions with cyclometalated phosphoramidite complexes bearing a dibenzocyclooctatetraene ligand: preparation of (π-allyl)Ir complexes and computational and NMR spectroscopic studies.

Authors:  Jevgenij A Raskatov; Mascha Jäkel; Bernd F Straub; Frank Rominger; Günter Helmchen
Journal:  Chemistry       Date:  2012-09-27       Impact factor: 5.236

Review 5.  Alzheimer's disease.

Authors:  Henry W Querfurth; Frank M LaFerla
Journal:  N Engl J Med       Date:  2010-01-28       Impact factor: 91.245

6.  Sequence determinants of enhanced amyloidogenicity of Alzheimer A{beta}42 peptide relative to A{beta}40.

Authors:  Woojin Kim; Michael H Hecht
Journal:  J Biol Chem       Date:  2005-08-03       Impact factor: 5.157

7.  C-terminal turn stability determines assembly differences between Aβ40 and Aβ42.

Authors:  Robin Roychaudhuri; Mingfeng Yang; Atul Deshpande; Gregory M Cole; Sally Frautschy; Aleksey Lomakin; George B Benedek; David B Teplow
Journal:  J Mol Biol       Date:  2012-11-12       Impact factor: 5.469

8.  Amyloid beta -protein (Abeta) assembly: Abeta 40 and Abeta 42 oligomerize through distinct pathways.

Authors:  Gal Bitan; Marina D Kirkitadze; Aleksey Lomakin; Sabrina S Vollers; George B Benedek; David B Teplow
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-27       Impact factor: 11.205

9.  Aβ(1-42) fibril structure illuminates self-recognition and replication of amyloid in Alzheimer's disease.

Authors:  Yiling Xiao; Buyong Ma; Dan McElheny; Sudhakar Parthasarathy; Fei Long; Minako Hoshi; Ruth Nussinov; Yoshitaka Ishii
Journal:  Nat Struct Mol Biol       Date:  2015-05-04       Impact factor: 15.369

Review 10.  On the subject of rigor in the study of amyloid β-protein assembly.

Authors:  David B Teplow
Journal:  Alzheimers Res Ther       Date:  2013-08-27       Impact factor: 6.982

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