期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2012
卷号：109
期号：12
页码：4443-4448
DOI：10.1073/pnas.1111305109
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Wild-type, full-length (40- and 42-residue) amyloid {beta}-peptide (A{beta}) fibrils have been shown by a variety of magnetic resonance techniques to contain cross-{beta} structures in which the {beta}-sheets have an in-register parallel supramolecular organization. In contrast, recent studies of fibrils formed in vitro by the Asp23-to-Asn mutant of 40-residue A{beta} (D23N-A{beta}1-40), which is associated with early onset neurodegeneration, indicate that D23N-A{beta}1-40 fibrils can contain either parallel or antiparallel {beta}-sheets. We report a protocol for producing structurally pure antiparallel D23N-A{beta}1-40 fibril samples and a series of solid state nuclear magnetic resonance and electron microscopy measurements that lead to a specific model for the antiparallel D23N-A{beta}1-40 fibril structure. This model reveals how both parallel and antiparallel cross-{beta} structures can be constructed from similar peptide monomer conformations and stabilized by similar sets of interactions, primarily hydrophobic in nature. We find that antiparallel D23N-A{beta}1-40 fibrils are thermodynamically metastable with respect to conversion to parallel structures, propagate less efficiently than parallel fibrils in seeded fibril growth, and therefore must nucleate more efficiently than parallel fibrils in order to be observable. Experiments in neuronal cell cultures indicate that both antiparallel and parallel D23N-A{beta}1-40 fibrils are cytotoxic. Thus, our antiparallel D23N-A{beta}1-40 fibril model represents a specific "toxic intermediate" in the aggregation process of a disease-associated A{beta} mutant.
关键词：Alzheimer’s disease ; amyloid structure ; solid state NMR
