Atomic View of a Toxic Amyloid Small Oligomer
Howard Hughes Medical Institute · University of California, Los Angeles · +2 more institutions
Abstract
Amyloid diseases, including Alzheimer's, Parkinson's, and the prion conditions, are each associated with a particular protein in fibrillar form. These amyloid fibrils were long suspected to be the disease agents, but evidence suggests that smaller, often transient and polymorphic oligomers are the toxic entities. Here, we identify a segment of the amyloid-forming protein αB crystallin, which forms an oligomeric complex exhibiting properties of other amyloid oligomers: β-sheet-rich structure, cytotoxicity, and recognition by an oligomer-specific antibody. The x-ray-derived atomic structure of the oligomer reveals a cylindrical barrel, formed from six antiparallel protein strands, that we term a cylindrin. The…
Citation impact
- FWCI
- 39.60
- Percentile
- 100%
- References
- 81
Authors
13- ALArthur LaganowskyCorresponding
Howard Hughes Medical Institute, University of California, Los Angeles
- CLCong Liu
Howard Hughes Medical Institute, University of California, Los Angeles
- MSM.R. Sawaya
Howard Hughes Medical Institute, University of California, Los Angeles
- JPJulian P. Whitelegge
Neuropsychiatric Research Institute
- JPJiyong Park
Howard Hughes Medical Institute, University of California, Los Angeles
Topics & keywords
- Oligomer
- Antiparallel (mathematics)
- Fibril
- Amyloid (mycology)
- Barrel (horology)
- Chemistry
- Amyloid fibril
- Biophysics
- Life in Land