𝔖 Bobbio Scriptorium
✦   LIBER   ✦

BACE1 interacts with lipid raft proteins

✍ Scribed by Chinatsu Hattori; Masashi Asai; Hayato Onishi; Noboru Sasagawa; Yasuhiro Hashimoto; Takaomi C. Saido; Kei Maruyama; Shigehiko Mizutani; Shoichi Ishiura


Book ID
102386375
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
248 KB
Volume
84
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A neuropathological hallmark of Alzheimer's disease is the presence of amyloid plaques in the brain. Amyloid‐β peptide (Aβ) is the major constituent of the plaques and is generated by proteolytic cleavages of amyloid precursor protein (APP) by β‐ and γ‐secretases. Growing evidence shows that lipid rafts are critically involved in regulating the Aβ generation. In support of this, APP, Aβ, and presenilins have been found in lipid rafts. Although cholesterol plays a crucial role in maintaining lipid rafts, functions of other components in the generation of Aβ are unknown. Caveolins (CAVs) and flotillins (FLOTs) are principal proteins related to lipid rafts and have been suggested to be involved in APP processing. Here, we report that FLOT‐1 binds to BACE1 (beta‐site APP cleaving enzyme 1) and that overexpression of CAV‐1 or FLOT‐1 results in recruiting BACE1 into lipid rafts and influence on β‐secretase activity in cultured cells. Our results show that both CAV‐1 and FLOT‐1 may modulate β‐secretase activity by interacting with BACE1. © 2006 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Inhibition by KMI-574 leads to dislocali
✍ Maiko Ebina; Eugene Futai; Chiaki Tanabe; Noboru Sasagawa; Yoshiaki Kiso; Shoich 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 278 KB

## Abstract BACE1 initiates processing of the amyloid precursor protein (APP) in the production of amyloid β (Aβ) peptide. After β‐cleavage by BACE1, the C‐terminal stub of the APP fragment is further processed by the γ‐secretase complex to produce Aβ. Because APP, Aβ, the γ‐secretase complex, and

The low-density lipoprotein receptor-rel
✍ Lihua Wu; Steven L. Gonias 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 294 KB

## Abstract The low‐density lipoprotein receptor‐related protein‐1 (LRP‐1) is a multifunctional receptor that undergoes constitutive endocytosis and recycling. To identify LRP‐1 in lipid rafts, we biotin‐labeled cells using a membrane‐impermeable reagent and prepared Triton X‐100 fractions. Raft‐as