ISSN:
1420-9071
Keywords:
Key words. Amyloid; amyloidosis; fibrils; protofilaments; Alzheimer's disease; spongiform encephalopathies; fibre diffraction; cross-β conformation.
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
,
Medicine
Notes:
Abstract. Amyloidoses are diseases, including some currently prominent such as Alzheimer's disease, bovine spongiform encephalophaty (BSE) and Type II diabetes, in which soluble proteins are deposited in a specific, highly stable, fibrillar form. The amyloid fibrils are made up of protofilaments whose molecular structure is composed of pairs of β-sheets in a helical form that allows them to be continuously hydrogen-bonded along the length of the fibril. The observation that similar fibrils are generated from different proteins indicates that fibril formation is accompanied by structural conversion. The transmissible spongiform encephalopathies, such as BSE and kuru, involve an infectious agent identified with the prion protein. The properties of the agent are more consistent with prion amyloid than the protein itself, suggesting infectivity in these diseases is equivalent to the 'seeding' of amyloid fibrils at a new site.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/s000180050107
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