The structural biology of protein aggregation diseases: Fundamental questions and some answers

被引:146
作者
Eisenberg, David [1 ]
Nelson, Rebecca
Sawaya, Michael R.
Balbirnie, Melinda
Sambashivan, Shilpa
Ivanova, Magdalena I.
Madsen, Anders O.
Riekel, Christian
机构
[1] Univ Calif Los Angeles, DOE Inst Genom & Proteom, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] Univ Copenhagen, KBH, Dept Chem, Ctr Crystallog Studies, DK-2100 Copenhagen, Denmark
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
关键词
D O I
10.1021/ar0500618
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amyloid fibrils are found in association with at least two dozen fatal diseases. The tendency of numerous proteins to convert into amyloid-like fibrils poses fundamental questions for structural biology and for protein science in general. Among these are the following: What is the structure of the cross-beta spine, common to amyloid-like fibrils? Is there a sequence signature for proteins that form amyloid-like fibrils? What is the nature of the structural conversion from native to amyloid states, and do fibril-forming proteins have two distinct stable states, the native state and the amyloid state? What is the basis of protein complementarity, in which a protein chain can bind to itself? We offer tentative answers here, based on our own recent structural studies.
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页码:568 / 575
页数:8
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