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The structural evaluation of amyloid beta on lipid membranes
Author(s) -
Aoyagi Satoka,
Iwamura Miki,
Shimanouchi Toshinori,
Yokoyama Yuta,
Iwai Hideo
Publication year - 2016
Publication title -
surface and interface analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.52
H-Index - 90
eISSN - 1096-9918
pISSN - 0142-2421
DOI - 10.1002/sia.6086
Subject(s) - membrane , chemistry , secondary ion mass spectrometry , lipid bilayer , ion , peptide , principal component analysis , biophysics , phosphocholine , folding (dsp implementation) , analytical chemistry (journal) , mass spectrometry , chromatography , crystallography , biochemistry , phospholipid , organic chemistry , biology , artificial intelligence , phosphatidylcholine , computer science , electrical engineering , engineering
Amyloid beta (Aβ) adsorption onto lipid membranes depending on the condition of a lipid was investigated by means of time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS). Aβ aggregation depending on the different hardness of lipid membrane has not been clarified yet although it is important to understand Alzheimer's disease. Aβ (1–40) on three different lipid membranes having different transition temperatures has been evaluated using ToF‐SIMS in the previous study, and in this study, the differences between Aβ on liquid crystalline‐phase lipid membranes and that on gel‐phase lipid membranes were investigated in order to clarify the mechanisms of aggregation and peptide folding change. ToF‐SIMS secondary ion images clearly showed Aβ distribution on lipid membranes. Because ToF‐SIMS data is extremely complicated although it contains rich information, it was analysed by principal component analysis (PCA). Score images indicated by PCA are consistent with the images of secondary ions related to Aβ and are clearer than the secondary ion images. Moreover, PCA results suggest the difference between Aβ on different lipid membranes in terms of amino acid fragment ions, and the orientation of Aβ on 1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphocholine was indicated. Copyright © 2016 John Wiley & Sons, Ltd.