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Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics

The neuroprotective E3-ubiquitin ligase CHIP is linked to healthy aging. Here, we present a protocol using a patient-derived iPSC line with a triplication of the α-synuclein gene to produce gene-edited cells isogenic for CHIP. We describe iPSC differentiation into cortical neurons and their identity...

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Detalles Bibliográficos
Autores principales: Dias, Catarina, Nita, Erisa, Faktor, Jakub, Hernychova, Lenka, Kunath, Tilo, Ball, Kathryn L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980993/
https://www.ncbi.nlm.nih.gov/pubmed/35391935
http://dx.doi.org/10.1016/j.xpro.2022.101247
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author Dias, Catarina
Nita, Erisa
Faktor, Jakub
Hernychova, Lenka
Kunath, Tilo
Ball, Kathryn L.
author_facet Dias, Catarina
Nita, Erisa
Faktor, Jakub
Hernychova, Lenka
Kunath, Tilo
Ball, Kathryn L.
author_sort Dias, Catarina
collection PubMed
description The neuroprotective E3-ubiquitin ligase CHIP is linked to healthy aging. Here, we present a protocol using a patient-derived iPSC line with a triplication of the α-synuclein gene to produce gene-edited cells isogenic for CHIP. We describe iPSC differentiation into cortical neurons and their identity validation. We then detail mass spectrometry-based approaches (SWATH-MS) to identify dominant changes in the steady state proteome generated by loss of CHIP function. This protocol can be adapted to other proteins that impact proteostasis in neurons. For complete details on the use and execution of this protocol, please refer to Dias et al. (2021).
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spelling pubmed-89809932022-04-06 Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics Dias, Catarina Nita, Erisa Faktor, Jakub Hernychova, Lenka Kunath, Tilo Ball, Kathryn L. STAR Protoc Protocol The neuroprotective E3-ubiquitin ligase CHIP is linked to healthy aging. Here, we present a protocol using a patient-derived iPSC line with a triplication of the α-synuclein gene to produce gene-edited cells isogenic for CHIP. We describe iPSC differentiation into cortical neurons and their identity validation. We then detail mass spectrometry-based approaches (SWATH-MS) to identify dominant changes in the steady state proteome generated by loss of CHIP function. This protocol can be adapted to other proteins that impact proteostasis in neurons. For complete details on the use and execution of this protocol, please refer to Dias et al. (2021). Elsevier 2022-04-02 /pmc/articles/PMC8980993/ /pubmed/35391935 http://dx.doi.org/10.1016/j.xpro.2022.101247 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Dias, Catarina
Nita, Erisa
Faktor, Jakub
Hernychova, Lenka
Kunath, Tilo
Ball, Kathryn L.
Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title_full Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title_fullStr Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title_full_unstemmed Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title_short Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
title_sort generation of a chip isogenic human ipsc-derived cortical neuron model for functional proteomics
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980993/
https://www.ncbi.nlm.nih.gov/pubmed/35391935
http://dx.doi.org/10.1016/j.xpro.2022.101247
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