Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8299319 | Biochimica et Biophysica Acta (BBA) - Biomembranes | 2018 | 61 Pages |
Abstract
The toxic deposition of misfolded amyloidogenic proteins is associated with more than fifty protein misfolding diseases (PMDs), including Alzheimer's disease, Parkinson's disease and type 2 diabetes mellitus. Protein deposition is a multi-step process modulated by a variety of factors, in particular by membrane-protein interaction. The interaction results in permeabilization of biomembranes contributing to the cytotoxicity that leads to PMDs. Different biological and physiochemical factors, such as protein sequence, lipid composition, and chaperones, are known to affect the membrane-protein interaction. Here, we provide a comprehensive review of the mechanisms and contributing factors of the interaction between biomembranes and amyloidogenic proteins, and a summary of the therapeutic approaches to PMDs that target this interaction. This article is part of a Special Issue entitled: Protein Aggregation and Misfolding at the Cell Membrane Interface edited by Ayyalusamy Ramamoorthy.
Keywords
DMPGdHPCFAPPoPCdMPCIAPPDOPSCysDOPCDPPCDOPGDOTAPAβPMDSPOPAHDLDLPCDPPGCCBSDSCHOLPOPGPTM1,2-dilauroyl-sn-glycero-3-phosphocholine1,2-dioleoyl-sn-glycero-3-phosphocholine1,2-dioleoyl-sn-glycero-3-phosphoethanolamine1,2-dipalmitoyl-sn-glycero-3-phosphocholine1,2-dihexanoyl-sn-glycero-3-phosphocholine1,2-dioleoyl-3-trimethylammonium-propaneFamilial amyloidotic polyneuropathyPOPssphingomyelinpost-translational modificationGraphene oxideamyloid betalarge unilamellar vesicleAlzheimer's diseaseParkinson's diseaseProtein misfolding diseasesBiomembraneTherapyblood brain barrierBBBsodium dodecyl sulphateCysteinephosphatidylinositolphosphatidylcholinephosphatidylglycerolphosphatidylethanolaminePhosphatidylserineLUVhigh density lipoproteinSUVCalcium channel blockerPOPEIslet amyloid polypeptideDOPEcholesterolSmall unilamellar vesicle
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Authors
Biao Cheng, Yang Li, Liang Ma, Zhuoyi Wang, Robert B. Petersen, Ling Zheng, Yuchen Chen, Kun Huang,