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Deformation of stable and toxic hIAPP oligomers by liposomes with distinct na-nomechanical features and re-duced cytotoxicity

Abstract

Human islet amyloid polypeptide (hIAPP) oligomers are transient due to rapid aggregation rate in vitro, but playing an important role in the pathogenesis of type 2 diabetes mellitus (T2DM). Here we report an easy and robust method to generate toxic hIAPP oligomers, which is stable for at least 8 hours. The toxic hIAPP oligomers quickly are transformed from α-helix to β-sheet by membrane phospholipid, 1, 2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes, exhibiting distinct nanomechanical features from the hIAPP oligomers or pristine fibrils. DOPC liposomes significantly block the cytotoxicity induced by the hIAPP oligomers, which has the potential for new treatment.

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Publication details

The article was received on 13 Aug 2019, accepted on 03 Nov 2019 and first published on 05 Nov 2019


Article type: Communication
DOI: 10.1039/C9CC06264E
Chem. Commun., 2019, Accepted Manuscript

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    Deformation of stable and toxic hIAPP oligomers by liposomes with distinct na-nomechanical features and re-duced cytotoxicity

    L. Zhang, Q. Chen, P. Li, L. Yuan, Y. Feng, J. Wang, X. Mao and L. Liu, Chem. Commun., 2019, Accepted Manuscript , DOI: 10.1039/C9CC06264E

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