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ACS Chem Neurosci. 2010 Apr 21;1(4):315-24. doi: 10.1021/cn900041x. Epub 2010 Feb 3.

Effects of Congo red on aβ(1-40) fibril formation process and morphology.

Author information

1
Department of Biochemistry and Organic Chemistry, Uppsala University, Box 576, S-75123 Uppsala, Sweden.

Abstract

Alzheimer's disease (AD), an age-related neurodegenerative disorder, is the most common form of dementia, and the seventh-leading cause of death in the United States. Current treatments offer only symptomatic relief; thus, there is a great need for new treatments with disease-modifying potential. One pathological hallmark of AD is so-called senile plaques, mainly made up of β-sheet-rich assemblies of 40- or 42-residue amyloid β-peptides (Aβ). Hence, inhibition of Aβ aggregation is actively explored as an option to prevent or treat AD. Congo red (CR) has been widely used as a model antiamyloid agent to prevent Aβ aggregation. Herein, we report detailed morphological studies on the effect of CR as an antiamyloid agent, by circular dichroism spectroscopy, photo-induced cross-linking reactions, and atomic force microscopy. We also demonstrate the effect of CR on a preaggregated sample of Aβ(1-40). Our result suggests that Aβ(1-40) follows a different path for aggregation in the presence of CR.

KEYWORDS:

Alzheimer’s disease; Congo red; aggregates; amyloid; amyloid β-peptide; atomic force microscopy; fibrils; oligomers

PMID:
22778828
PMCID:
PMC3368672
DOI:
10.1021/cn900041x
[Indexed for MEDLINE]
Free PMC Article

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