Amyloïd beta peptide, one of the main components of Alzheimer's disease, is derived from the proteolytic processing of its precursor beta-APP (Beta Amyloïd Precursor Protein). This amyloïdogenic pathway involves two proteolytic activities: beta- and gamma-secretase. The gamma-secretase activity is carried by a macro-molecular complex composed...
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December 1, 2008 (v1)PublicationUploaded on: December 4, 2022
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July 2009 (v1)Journal articlePharmacological evidences for DFK167-sensitive presenilin-independent gamma-secretase-like activity.
Amyloid-beta (Abeta) peptides production is thought to be a key event in the neurodegenerative process ultimately leading to Alzheimer's disease (AD) pathology. A bulk of studies concur to propose that the C-terminal moiety of Abeta is released from its precursor beta-amyloid precursor protein by a high molecular weight enzymatic complex...
Uploaded on: December 3, 2022 -
April 11, 2008 (v1)Journal article
Beta-amyloid (Abeta) peptides that accumulate in Alzheimer disease are generated from the beta-amyloid precursor protein (betaAPP) by cleavages by beta-secretase BACE1 and by presenilin-dependent gamma-secretase activities. Very few data document a putative cross-talk between these proteases and the regulatory mechanisms underlying such...
Uploaded on: December 4, 2022 -
April 2009 (v1)Journal article
Several lines of data previously indicated that N-terminally truncated forms of amyloid-beta (Abeta) peptides are likely the earliest and more abundant species immunohistochemically detectable in Alzheimer's disease-affected brains. It is noteworthy that the free N-terminal residue of full-length Abeta (fl-Abeta) is an aspartyl residue,...
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April 2007 (v1)Journal article
The presenilin-dependent gamma-secretase activity, which is responsible for the generation of amyloid beta-peptide, is a high molecular weight complex composed of at least four components, namely, presenilin-1 (or presenilin-2), nicastrin, Aph-1, and Pen-2. Previous data indicated that presenilins, which are thought to harbor the catalytic core...
Uploaded on: February 28, 2023 -
January 1, 2012 (v1)Journal article
One of the major pathological hallmarks of brains affected with Alzheimer's disease (AD) is the senile plaque, an extracellular deposit mainly composed of a set of highly insoluble peptides of various lengths (39-43 amino acids) referred to as amyloid-β (Aβ) peptides. Aβ peptides are derived from combined proteolytic cleavages undergone on the...
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June 20, 2008 (v1)Journal article
The presenilin (PS)-dependent gamma-secretase activity refers to a high molecular mass-complex including, besides PS1 or PS2, three other proteins recently identified, namely nicastrin, Aph-1, and Pen-2. This proteolytic complex has been shown to contribute to both gamma- and epsilon-cleavages of the beta-amyloid precursor protein (betaAPP),...
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September 1, 2007 (v1)Journal article
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Uploaded on: December 4, 2022 -
November 1, 2009 (v1)Journal article
The senile plaques found in the brains of patients with Alzheimer's disease are mainly due to the accumulation of amyloid beta-peptides (A beta) that are liberated by gamma-secretase, a high molecular weight complex including presenilins, PEN-2, APH-1 and nicastrin. The depletion of each of these proteins disrupts the complex assembly into a...
Uploaded on: December 4, 2022 -
June 12, 2009 (v1)Journal article
Complexes involved in the gamma/epsilon-secretase-regulated intramembranous proteolysis of substrates such as the amyloid-beta precursor protein are composed primarily of presenilin (PS1 or PS2), nicastrin, anterior pharynx defective-1 (APH1), and PEN2. The presenilin aspartyl residues form the catalytic site, and similar potentially functional...
Uploaded on: December 3, 2022