Study suggests another avenue for detecting Alzheimer’s
April 2nd, 2011 - 4:46 pm ICT by ANILondon, April 02 (ANI): A well-known chemical process called acetylation has a previously unrecognized association with one of the biological processes associated with Alzheimer’s disease and related disorders, researchers at the University of Pennsylvania School of Medicine have determined.
Tau is one of the primary disease proteins associated with a suite of neurodegenerative diseases. Tau proteins are expressed primarily in the central nervous system where they help with the assembly and stability of microtubules, protein structures that are the backbone of the nerve-cell communication system.
“Acetylation was only detected in diseased brain tissue from patients with Alzheimer’s disease or frontotemporal degeneration, suggesting it may have a role in tau transformation linked to disease onset and progression,” said senior author Virginia M.-Y. Lee, director of Penn’s Center for Neurodegenerative Disease Research.
“This suggests that one type of acetylation is a potential target for drug discovery and biomarker development for Alzheimer’s and related tauopathies.”
The researchers demonstrated that tau acetylation led to a loss of one of its major functions - to promote microtubule assembly, in addition to gaining a toxic function, pathological tau aggregation. Mass spectrometry analysis identified specific acetylation sites in the tau protein sequence that overlapped with known microtubule binding sequences, so acetylation may also play a role in faulty binding of tau to microtubules.
How normal tau becomes disengaged from microtubules to form disease-related clumps remains unknown. This study shows that acetylation is most likely another chemical modification implicated in neurodegenerative disorders to be explored as a potential way to detect and fight brain disease.
The findings have been published in the latest issue of Nature Communications. (ANI)
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Tags: brain disease, brain tissue, central nervous system, clumps, disease onset, diseased brain, drug discovery, mass spectrometry analysis, nerve cell communication, neurodegenerative diseases, neurodegenerative disorders, pennsylvania school, protein sequence, protein structures, s center, target, tau protein, tau proteins, university of pennsylvania, university of pennsylvania school of medicine