UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Extracellular interface between APP and Nicastrin regulates Aβ length and response to γ-secretase modulators

Petit, D; Hitzenberger, M; Lismont, S; Zoltowska, KM; Ryan, NS; Mercken, M; Bischoff, F; ... Chávez-Gutiérrez, L; + view all (2019) Extracellular interface between APP and Nicastrin regulates Aβ length and response to γ-secretase modulators. The EMBO Journal , Article e101494. 10.15252/embj.2019101494. (In press). Green open access

[thumbnail of Ryan_Extracellular interface between APP and Nicastrin regulates Aβ length and response to γ-secretase modulators_AOP.pdf]
Preview
Text
Ryan_Extracellular interface between APP and Nicastrin regulates Aβ length and response to γ-secretase modulators_AOP.pdf

Download (4MB) | Preview

Abstract

γ‐Secretase complexes (GSECs) are multimeric membrane proteases involved in a variety of physiological processes and linked to Alzheimer's disease (AD). Presenilin (PSEN, catalytic subunit), Nicastrin (NCT), Presenilin Enhancer 2 (PEN‐2), and Anterior Pharynx Defective 1 (APH1) are the essential subunits of GSECs. Mutations in PSEN and the Amyloid Precursor Protein (APP) cause early‐onset AD. GSECs successively cut APP to generate amyloid‐β (Aβ) peptides of various lengths. AD‐causing mutations destabilize GSEC‐APP/Aβ_{n} interactions and thus enhance the production of longer Aβs, which elicit neurotoxic events underlying pathogenesis. Here, we investigated the molecular strategies that anchor GSEC and APP/Aβ_{n} during the sequential proteolysis. Our studies reveal that a direct interaction between NCT ectodomain and APP_{C99} influences the stability of GSEC‐Aβn assemblies and thereby modulates Aβ length. The data suggest a potential link between single‐nucleotide variants in NCSTN and AD risk. Furthermore, our work indicates that an extracellular interface between the protease (NCT, PSEN) and the substrate (APP) represents the target for compounds (GSMs) modulating Aβ length. Our findings may guide future rationale‐based drug discovery efforts.

Type: Article
Title: Extracellular interface between APP and Nicastrin regulates Aβ length and response to γ-secretase modulators
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.15252/embj.2019101494
Publisher version: http://dx.doi.org/10.15252/embj.2019101494
Language: English
Additional information: © 2019 The Authors. Published under the terms of the CC BY NC ND 4.0 license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Alzheimer's disease, Nicastrin, amyloid‐beta, γ‐secretase, γ‐secretase modulators
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10075676
Downloads since deposit
72Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item