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Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids

Characterization of cerebral organoids has been challenging due to their heterogeneous nature. Here, we optimized a protocol to streamline the generation of FACS-purified cell populations from human cerebral organoids for proteomic analysis with liquid chromatography tandem mass spectrometry (LC-MS/...

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Detalles Bibliográficos
Autores principales: Melliou, Sofia, Diamandis, Phedias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597183/
https://www.ncbi.nlm.nih.gov/pubmed/36313540
http://dx.doi.org/10.1016/j.xpro.2022.101774
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author Melliou, Sofia
Diamandis, Phedias
author_facet Melliou, Sofia
Diamandis, Phedias
author_sort Melliou, Sofia
collection PubMed
description Characterization of cerebral organoids has been challenging due to their heterogeneous nature. Here, we optimized a protocol to streamline the generation of FACS-purified cell populations from human cerebral organoids for proteomic analysis with liquid chromatography tandem mass spectrometry (LC-MS/MS). We describe the procedures for enzymatic dissociation of organoids into single-cell suspension, the generation of cell-type-specific lysates, peptide extraction, and proteomic analysis. This generalizable approach can be used to study temporal and cell-type-specific protein dynamics in developing cerebral organoids. For complete details on the use and execution of this protocol, please refer to Melliou et al. (2022).
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spelling pubmed-95971832022-10-27 Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids Melliou, Sofia Diamandis, Phedias STAR Protoc Protocol Characterization of cerebral organoids has been challenging due to their heterogeneous nature. Here, we optimized a protocol to streamline the generation of FACS-purified cell populations from human cerebral organoids for proteomic analysis with liquid chromatography tandem mass spectrometry (LC-MS/MS). We describe the procedures for enzymatic dissociation of organoids into single-cell suspension, the generation of cell-type-specific lysates, peptide extraction, and proteomic analysis. This generalizable approach can be used to study temporal and cell-type-specific protein dynamics in developing cerebral organoids. For complete details on the use and execution of this protocol, please refer to Melliou et al. (2022). Elsevier 2022-10-21 /pmc/articles/PMC9597183/ /pubmed/36313540 http://dx.doi.org/10.1016/j.xpro.2022.101774 Text en © 2022 The Author(s) 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
Melliou, Sofia
Diamandis, Phedias
Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title_full Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title_fullStr Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title_full_unstemmed Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title_short Generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
title_sort generation of cell-type-specific proteomes of neurodevelopment from human cerebral organoids
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597183/
https://www.ncbi.nlm.nih.gov/pubmed/36313540
http://dx.doi.org/10.1016/j.xpro.2022.101774
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