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Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry

Cerebrospinal fluid (CSF) is a biofluid in direct contact with the brain and as such constitutes a sample of choice in neurological disorder research, including neurodegenerative diseases such as Alzheimer or Parkinson. Human CSF has still been less studied using proteomic technologies compared to o...

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Detalles Bibliográficos
Autores principales: Macron, Charlotte, Lavigne, Regis, Núñez Galindo, Antonio, Affolter, Michael, Pineau, Charles, Dayon, Loïc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251648/
https://www.ncbi.nlm.nih.gov/pubmed/32478154
http://dx.doi.org/10.1016/j.dib.2020.105704
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author Macron, Charlotte
Lavigne, Regis
Núñez Galindo, Antonio
Affolter, Michael
Pineau, Charles
Dayon, Loïc
author_facet Macron, Charlotte
Lavigne, Regis
Núñez Galindo, Antonio
Affolter, Michael
Pineau, Charles
Dayon, Loïc
author_sort Macron, Charlotte
collection PubMed
description Cerebrospinal fluid (CSF) is a biofluid in direct contact with the brain and as such constitutes a sample of choice in neurological disorder research, including neurodegenerative diseases such as Alzheimer or Parkinson. Human CSF has still been less studied using proteomic technologies compared to other biological fluids such as blood plasma or serum. In this work, a pool of “normal” human CSF samples was analysed using a shotgun proteomic workflow that combined removal of highly abundant proteins by immunoaffinity depletion and isoelectric focussing fractionation of tryptic peptides to alleviate the complexity of the biofluid. The resulting 24 fractions were analysed using liquid chromatography coupled to a high-resolution and high-accuracy timsTOF Pro mass spectrometer. This state-of-the-art mass spectrometry-based proteomic workflow allowed the identification of 3’174 proteins in CSF. The dataset reported herein completes the pool of the most comprehensive human CSF proteomes obtained so far. An overview of the identified proteins is provided based on gene ontology annotation. Mass and tandem mass spectra are made available as a possible starting point for further studies exploring the human CSF proteome.
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spelling pubmed-72516482020-05-29 Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry Macron, Charlotte Lavigne, Regis Núñez Galindo, Antonio Affolter, Michael Pineau, Charles Dayon, Loïc Data Brief Proteomics Cerebrospinal fluid (CSF) is a biofluid in direct contact with the brain and as such constitutes a sample of choice in neurological disorder research, including neurodegenerative diseases such as Alzheimer or Parkinson. Human CSF has still been less studied using proteomic technologies compared to other biological fluids such as blood plasma or serum. In this work, a pool of “normal” human CSF samples was analysed using a shotgun proteomic workflow that combined removal of highly abundant proteins by immunoaffinity depletion and isoelectric focussing fractionation of tryptic peptides to alleviate the complexity of the biofluid. The resulting 24 fractions were analysed using liquid chromatography coupled to a high-resolution and high-accuracy timsTOF Pro mass spectrometer. This state-of-the-art mass spectrometry-based proteomic workflow allowed the identification of 3’174 proteins in CSF. The dataset reported herein completes the pool of the most comprehensive human CSF proteomes obtained so far. An overview of the identified proteins is provided based on gene ontology annotation. Mass and tandem mass spectra are made available as a possible starting point for further studies exploring the human CSF proteome. Elsevier 2020-05-16 /pmc/articles/PMC7251648/ /pubmed/32478154 http://dx.doi.org/10.1016/j.dib.2020.105704 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Proteomics
Macron, Charlotte
Lavigne, Regis
Núñez Galindo, Antonio
Affolter, Michael
Pineau, Charles
Dayon, Loïc
Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title_full Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title_fullStr Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title_full_unstemmed Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title_short Exploration of human cerebrospinal fluid: A large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
title_sort exploration of human cerebrospinal fluid: a large proteome dataset revealed by trapped ion mobility time-of-flight mass spectrometry
topic Proteomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251648/
https://www.ncbi.nlm.nih.gov/pubmed/32478154
http://dx.doi.org/10.1016/j.dib.2020.105704
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