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A gorge-spanning, high-affinity cholinesterase inhibitor to explore beta-amyloid plaques.

作者信息

Elsinghorst Paul W, Härtig Wolfgang, Goldhammer Simone, Grosche Jens, Gütschow Michael

机构信息

Pharmaceutical Institute, Pharmaceutical Chemistry I, University of Bonn, An der Immenburg 4, D-53121, Bonn, Germany.

出版信息

Org Biomol Chem. 2009 Oct 7;7(19):3940-6. doi: 10.1039/b909612d. Epub 2009 Jul 17.

DOI:10.1039/b909612d
PMID:19763296
Abstract

Cholinesterases are involved in the pathological formation of beta-amyloid plaques. To investigate this pathohistological hallmark of Alzheimer's disease we prepared a high-affinity, fluorescent cholinesterase inhibitor. Its fluorescence intensity was significantly enhanced upon binding to cholinesterases. Using this probe, brain samples from mice and humans affected by Alzheimer's disease were successfully analyzed for beta-amyloid plaques. Unexpectedly, it was discovered, by competition experiments, that the compound binds to amyloid structures, rather than to cholinesterases inside of the plaques.

摘要

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