8IM7

Human gamma-secretase treated with ganglioside GM1

8IM7 の概要

• エントリーDOI: 10.2210/pdb8im7/pdb
• EMDBエントリー: 35572
• 分子名称: Nicastrin, Presenilin-1 CTF12, Gamma-secretase subunit APH-1A, ... (9 entities in total)
• 機能のキーワード: intramembrane protease, lipid, ganglioside, gm1, membrane protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 178966.75

構造登録者

Zhou, R.,Yang, G.,Shi, Y. (登録日: 2023-03-06, 公開日: 2024-01-17, 最終更新日: 2025-07-23)

主引用文献

Wang, X.,Zhou, R.,Sun, X.,Li, J.,Wang, J.,Yue, W.,Wang, L.,Liu, H.,Shi, Y.,Zhang, D.
Preferential Regulation of Gamma-Secretase-Mediated Cleavage of APP by Ganglioside GM1 Reveals a Potential Therapeutic Target for Alzheimer's Disease.
Adv Sci, 10:e2303411-e2303411, 2023

PubMed Abstract: A hallmark of Alzheimer's disease (AD) is the senile plaque, which contains β-amyloid peptides (Aβ). Ganglioside GM1 is the most common brain ganglioside. However, the mechanism of GM1 in modulating Aβ processing is rarely known. Aβ levels are detected by using Immunohistochemistry (IHC) and enzyme-linked immune-sorbent assay (ELISA). Cryo-electron microscopy (Cryo-EM) is used to determine the structure of γ-secretase supplemented with GM1. The levels of the cleavage of amyloid precursor protein (APP)/Cadherin/Notch1 are detected using Western blot analysis. Y maze, object translocation, and Barnes maze are performed to evaluate cognitive functions. GM1 leads to conformational change of γ-secretase structure and specifically accelerates γ-secretase cleavage of APP without affecting other substrates including Notch1, potentially through its interaction with the N-terminal fragment of presenilin 1 (PS1). Reduction of GM1 levels decreases amyloid plaque deposition and improves cognitive dysfunction. This study reveals the mechanism of GM1 in Aβ generation and provides the evidence that decreasing GM1 levels represents a potential strategy in AD treatment. These results provide insights into the detailed mechanism of the effect of GM1 on PS1, representing a step toward the characterization of its novel role in the modulation of γ-secretase activity and the pathogenesis of AD.

PubMed: 37759382
DOI: 10.1002/advs.202303411

実験手法

ELECTRON MICROSCOPY (3.4 Å)