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A11-positive β-amyloid Oligomer Preparation and Assessment Using Dot Blotting Analysis
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Ultrafiltrate of blood plasma modulates amyloid-β aggregation

Aleksandra Nowicka1, Andrzej A Szczepankiewicz, Andrzej Jaklewicz

  • 1Warsaw University of Life Sciences - SGGW, Warsaw, Poland.

Journal of Alzheimer'S Disease : JAD
|October 9, 2010
PubMed

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Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...