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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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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. |
format | Online Article Text |
id | pubmed-6442608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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