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GSAP modulates γ-secretase specificity by inducing conformational change in PS1

The mechanism by which γ-secretase activating protein (GSAP) regulates γ-secretase activity has not yet been elucidated. Here, we show that knockout of GSAP in cultured cells directly reduces γ-secretase activity for Aβ production, but not for Notch1 cleavage, suggesting that GSAP may induce a confo...

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Autores principales: Wong, Eitan, Liao, George P., Chang, Jerry C., Xu, Peng, Li, Yue-Ming, Greengard, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442608/
https://www.ncbi.nlm.nih.gov/pubmed/30850537
http://dx.doi.org/10.1073/pnas.1820160116
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author Wong, Eitan
Liao, George P.
Chang, Jerry C.
Xu, Peng
Li, Yue-Ming
Greengard, Paul
author_facet Wong, Eitan
Liao, George P.
Chang, Jerry C.
Xu, Peng
Li, Yue-Ming
Greengard, Paul
author_sort Wong, Eitan
collection PubMed
description The mechanism by which γ-secretase activating protein (GSAP) regulates γ-secretase activity has not yet been elucidated. Here, we show that knockout of GSAP in cultured cells directly reduces γ-secretase activity for Aβ production, but not for Notch1 cleavage, suggesting that GSAP may induce a conformational change contributing to the specificity of γ-secretase. Furthermore, using an active-site–directed photoprobe with double cross-linking moieties, we demonstrate that GSAP modifies the orientation and/or distance of the PS1 N-terminal fragment and the PS1 C-terminal fragment, a region containing the active site of γ-secretase. This work offers insight into how GSAP regulates γ-secretase specificity.
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spelling pubmed-64426082019-04-05 GSAP modulates γ-secretase specificity by inducing conformational change in PS1 Wong, Eitan Liao, George P. Chang, Jerry C. Xu, Peng Li, Yue-Ming Greengard, Paul Proc Natl Acad Sci U S A Biological Sciences The mechanism by which γ-secretase activating protein (GSAP) regulates γ-secretase activity has not yet been elucidated. Here, we show that knockout of GSAP in cultured cells directly reduces γ-secretase activity for Aβ production, but not for Notch1 cleavage, suggesting that GSAP may induce a conformational change contributing to the specificity of γ-secretase. Furthermore, using an active-site–directed photoprobe with double cross-linking moieties, we demonstrate that GSAP modifies the orientation and/or distance of the PS1 N-terminal fragment and the PS1 C-terminal fragment, a region containing the active site of γ-secretase. This work offers insight into how GSAP regulates γ-secretase specificity. National Academy of Sciences 2019-03-26 2019-03-08 /pmc/articles/PMC6442608/ /pubmed/30850537 http://dx.doi.org/10.1073/pnas.1820160116 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 Biological Sciences
Wong, Eitan
Liao, George P.
Chang, Jerry C.
Xu, Peng
Li, Yue-Ming
Greengard, Paul
GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title_full GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title_fullStr GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title_full_unstemmed GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title_short GSAP modulates γ-secretase specificity by inducing conformational change in PS1
title_sort gsap modulates γ-secretase specificity by inducing conformational change in ps1
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442608/
https://www.ncbi.nlm.nih.gov/pubmed/30850537
http://dx.doi.org/10.1073/pnas.1820160116
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