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• W1517177013 abstract "The elucidation of the structure of amyloid fibrils and related aggregates is an important step toward understanding the pathogenesis of diseases like Alzheimer's disease, which feature protein misfolding and/or aggregation. However, the large size, heterogeneous morphology, and poor solubility of amyloid-like fibrils make them resistant to high-resolution structure determination. Using amyloid fibrils and protofibrils of the Alzheimer's plaque peptide amyloid beta as examples, we describe here the use of hydrogen/deuterium exchange methods in conjunction with electrospray ionization mass spectrometry to determine regions of the peptide involved in beta-sheet network when it is incorporated into protein aggregates. The advantages of this method are low sample utilization and high speed. The basic methodology exploits the fact that protons either involved in H-bonded secondary structures or buried in a protein's core structure exchange more slowly with deuterium than do solvent-exposed and non-H-bonded protons. Details of all aspects of this methodology, including sample preparation, data acquisition, and data analysis, are described. These data provide insights into the structures of monomers, protofibrils, and fibrils and to the structural relations among these states." @default.
• W1517177013 created "2016-06-24" @default.
• W1517177013 creator A5019061554 @default.
• W1517177013 creator A5020224365 @default.
• W1517177013 creator A5065786876 @default.
• W1517177013 date "2006-01-01" @default.
• W1517177013 modified "2023-10-14" @default.
• W1517177013 title "Hydrogen/Deuterium Exchange Mass Spectrometry Analysis of Protein Aggregates" @default.
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• W1517177013 doi "https://doi.org/10.1016/s0076-6879(06)13008-6" @default.
• W1517177013 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17046395" @default.
• W1517177013 hasPublicationYear "2006" @default.
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