The What, Where, and How of γ-Secretase Complex Assembly

- Authors: Daniel R. Dries1, Gang Yu2
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View Affiliations Hide Affiliations1 Department of Neuroscience, The University of Texas Southwestern Medical Center, Dallas, TX 75390-9111, USA 2 Department of Neuroscience, The University of Texas Southwestern Medical Center, Dallas, TX 75390-9111, USA
- Source: Advances in Alzheimer's Research Volume 1 , pp 147-186
- Publication Date: November 2013
- Language: English


The What, Where, and How of γ-Secretase Complex Assembly, Page 1 of 1
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Here we discuss the biology of γ-secretase, an enigmatic enzyme complex that is responsible for the generation of the β-amyloid peptide that constitutes the amyloid plaques of Alzheimer's disease. We begin with a brief review on the processing of the amyloid precursor protein and a brief discussion on the family of enzymes involved in regulated intramembrane proteolysis, of which γ-secretase is a member. We then identify the four major components of the γ-secretase complex presenilin, nicastrin, Aph-1, and Pen-2 with a focus on the identification of each and the role that each plays in the maturation and activity of the complex. Next, we summarize the known subcellular locations of each γ-secretase component and the sites of γ-secretase activity, as defined by the production of β-amyloid. Finally, we close by synthesizing all of the included topics into an overarching model for the assembly and trafficking of the γ-secretase complex, which serves as a launching point for further questions into the biology and function of γ-secretase in Alzheimer's disease.
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