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Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein

Presenilin is the catalytic subunit of γ-secretase, a four-component intramembrane protease responsible for the generation of β-amyloid (Aβ) peptides. Over 200 Alzheimer’s disease-related mutations have been identified in presenilin 1 (PS1) and PS2. Here, we report that Bax-inhibitor 1 (BI1), an evo...

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Detalles Bibliográficos
Autores principales: Wu, Shenjie, Song, Wenqi, Wong, Catherine C. L., Shi, Yigong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320538/
https://www.ncbi.nlm.nih.gov/pubmed/30559186
http://dx.doi.org/10.1073/pnas.1810870116
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author Wu, Shenjie
Song, Wenqi
Wong, Catherine C. L.
Shi, Yigong
author_facet Wu, Shenjie
Song, Wenqi
Wong, Catherine C. L.
Shi, Yigong
author_sort Wu, Shenjie
collection PubMed
description Presenilin is the catalytic subunit of γ-secretase, a four-component intramembrane protease responsible for the generation of β-amyloid (Aβ) peptides. Over 200 Alzheimer’s disease-related mutations have been identified in presenilin 1 (PS1) and PS2. Here, we report that Bax-inhibitor 1 (BI1), an evolutionarily conserved transmembrane protein, stably associates with PS1. BI1 specifically interacts with PS1 in isolation, but not with PS1 in the context of an assembled γ-secretase. The PS1–BI1 complex exhibits no apparent proteolytic activity, as judged by the inability to produce Aβ40 and Aβ42 from the substrate APP-C99. At an equimolar concentration, BI1 has no impact on the proteolytic activity of γ-secretase; at a 200-fold molar excess, BI1 reduces γ-secretase activity nearly by half. Our biochemical study identified BI1 as a PS1-interacting protein, suggesting additional functions of PS1 beyond its involvement in γ-secretase.
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spelling pubmed-63205382019-01-09 Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein Wu, Shenjie Song, Wenqi Wong, Catherine C. L. Shi, Yigong Proc Natl Acad Sci U S A PNAS Plus Presenilin is the catalytic subunit of γ-secretase, a four-component intramembrane protease responsible for the generation of β-amyloid (Aβ) peptides. Over 200 Alzheimer’s disease-related mutations have been identified in presenilin 1 (PS1) and PS2. Here, we report that Bax-inhibitor 1 (BI1), an evolutionarily conserved transmembrane protein, stably associates with PS1. BI1 specifically interacts with PS1 in isolation, but not with PS1 in the context of an assembled γ-secretase. The PS1–BI1 complex exhibits no apparent proteolytic activity, as judged by the inability to produce Aβ40 and Aβ42 from the substrate APP-C99. At an equimolar concentration, BI1 has no impact on the proteolytic activity of γ-secretase; at a 200-fold molar excess, BI1 reduces γ-secretase activity nearly by half. Our biochemical study identified BI1 as a PS1-interacting protein, suggesting additional functions of PS1 beyond its involvement in γ-secretase. National Academy of Sciences 2019-01-02 2018-12-17 /pmc/articles/PMC6320538/ /pubmed/30559186 http://dx.doi.org/10.1073/pnas.1810870116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Wu, Shenjie
Song, Wenqi
Wong, Catherine C. L.
Shi, Yigong
Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title_full Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title_fullStr Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title_full_unstemmed Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title_short Bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
title_sort bax inhibitor 1 is a γ-secretase–independent presenilin-binding protein
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320538/
https://www.ncbi.nlm.nih.gov/pubmed/30559186
http://dx.doi.org/10.1073/pnas.1810870116
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