Structural models of amyloid-like fibrils

被引:168
作者
Nelson, Rebecca [1 ]
Eisenberg, David [1 ]
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, US DOE, Inst Genom & Proteom, Los Angeles, CA 90095 USA
来源
FIBROUS PROTEINS: AMYLOIDS, PRIONS AND BETA PROTEINS | 2006年 / 73卷
关键词
D O I
10.1016/S0065-3233(06)73008-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amyloid fibrils are elongated, insoluble protein aggregates deposited in vivo in amyloid diseases, and amyloid-like fibrils are formed in vitro from soluble proteins. Both of these groups of fibrils, despite differences in the sequence and native structure of their component proteins, share common properties, including their core structure. Multiple models have been proposed for the common core structure, but in most cases, atomic-level structural details have yet to be determined. Here we review several structural models proposed for amyloid and amyloid-like fibrils and relate features of these models to the common fibril properties. We divide models into three classes: Refolding, Gain-of-Interaction, and Natively Disordered. The Refolding models propose structurally distinct native and fibrillar states and suggest that backbone interactions drive fibril formation. In contrast, the Gain-of-Interaction models propose a largely native-like structure for the protein in the fibril and highlight the importance of specific sequences in fibril formation. The Natively Disordered models have aspects in common with both Refolding and Gain-of-Interaction models. While each class of model suggests explanations for some of the common fibril properties, and some models, such as Gain-of-Interaction models with a cross-beta spine, fit a wider range of properties than others, no one class provides a complete explanation for all amyloid fibril behavior.
引用
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页码:235 / +
页数:49
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