In silico analysis of the apolipoprotein E and the amyloid β peptide interaction: Misfolding induced by frustration of the salt bridge network

Jinghui Luo, Jean Didier Maréchal, Sebastian Wärmländer, Astrid Gräslund, Alex Perálvarez-Marín

Research output: Contribution to journalArticleResearchpeer-review

27 Citations (Scopus)

Abstract

The relationship between Apolipoprotein E (ApoE) and the aggregation processes of the amyloid β (Aβ) peptide has been shown to be crucial for Alzheimer's disease (AD). The presence of the ApoE4 isoform is considered to be a contributing risk factor for AD. However, the detailed molecular properties of ApoE4 interacting with the Aβ peptide are unknown, although various mechanisms have been proposed to explain the physiological and pathological role of this relationship. Here, computer simulations have been used to investigate the process of Aβ interaction with the N-terminal domain of the human ApoE isoforms (ApoE2, ApoE3 and ApoE4). Molecular docking combined with molecular dynamics simulations have been undertaken to determine the Aβ peptide binding sites and the relative stability of binding to each of the ApoE isoforms. Our results show that from the several ApoE isoforms investigated, only ApoE4 presents a misfolded intermediate when bound to Aβ. Moreover, the initial a-helix used as the Aβ peptide model structure also becomes unstructured due to the interaction with ApoE4. These structural changes appear to be related to a rearrangement of the salt bridge network in ApoE4, for which we propose a model. It seems plausible that ApoE4 in its partially unfolded state is incapable of performing the clearance of Aβ, thereby promoting amyloid forming processes. Hence, the proposed model can be used to identify potential drug binding sites in the ApoE4-Aβ complex, where the interaction between the two molecules can be inhibited. © 2010 Luo et al.
Original languageEnglish
Article numbere1000663
JournalPLoS Computational Biology
Volume6
Issue number2
DOIs
Publication statusPublished - 1 Feb 2010

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