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Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis
Small extracellular vesicles have been intensively studied as a source of biomarkers in neurodegenerative disorders. The possibility to isolate neuron-derived small extracellular vesicles (NDsEV) from blood represents a potential window into brain pathological processes. To date, the absence of sens...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999506/ https://www.ncbi.nlm.nih.gov/pubmed/33799461 http://dx.doi.org/10.3390/ijms22062951 |
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author | Anastasi, Federica Masciandaro, Silvia Maria Carratore, Renata Del Dell’Anno, Maria Teresa Signore, Giovanni Falleni, Alessandra McDonnell, Liam A. Bongioanni, Paolo |
author_facet | Anastasi, Federica Masciandaro, Silvia Maria Carratore, Renata Del Dell’Anno, Maria Teresa Signore, Giovanni Falleni, Alessandra McDonnell, Liam A. Bongioanni, Paolo |
author_sort | Anastasi, Federica |
collection | PubMed |
description | Small extracellular vesicles have been intensively studied as a source of biomarkers in neurodegenerative disorders. The possibility to isolate neuron-derived small extracellular vesicles (NDsEV) from blood represents a potential window into brain pathological processes. To date, the absence of sensitive NDsEV isolation and full proteome characterization methods has meant their protein content has been underexplored, particularly for individual patients. Here, we report a rapid method based on an immunoplate covalently coated with mouse monoclonal anti-L1CAM antibody for the isolation and the proteome characterization of plasma-NDsEV from individual Parkinson’s disease (PD) patients. We isolated round-shaped vesicles with morphological characteristics consistent with exosomes. On average, 349 ± 38 protein groups were identified by liquid chromatography–tandem mass spectrometry (LC-MS/MS) analysis, 20 of which are annotated in the Human Protein Atlas as being highly expressed in the brain, and 213 were shared with a reference NDsEV dataset obtained from cultured human neurons. Moreover, this approach enabled the identification of 23 proteins belonging to the Parkinson disease KEGG pathway, as well as proteins previously reported as PD circulating biomarkers. |
format | Online Article Text |
id | pubmed-7999506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79995062021-03-28 Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis Anastasi, Federica Masciandaro, Silvia Maria Carratore, Renata Del Dell’Anno, Maria Teresa Signore, Giovanni Falleni, Alessandra McDonnell, Liam A. Bongioanni, Paolo Int J Mol Sci Article Small extracellular vesicles have been intensively studied as a source of biomarkers in neurodegenerative disorders. The possibility to isolate neuron-derived small extracellular vesicles (NDsEV) from blood represents a potential window into brain pathological processes. To date, the absence of sensitive NDsEV isolation and full proteome characterization methods has meant their protein content has been underexplored, particularly for individual patients. Here, we report a rapid method based on an immunoplate covalently coated with mouse monoclonal anti-L1CAM antibody for the isolation and the proteome characterization of plasma-NDsEV from individual Parkinson’s disease (PD) patients. We isolated round-shaped vesicles with morphological characteristics consistent with exosomes. On average, 349 ± 38 protein groups were identified by liquid chromatography–tandem mass spectrometry (LC-MS/MS) analysis, 20 of which are annotated in the Human Protein Atlas as being highly expressed in the brain, and 213 were shared with a reference NDsEV dataset obtained from cultured human neurons. Moreover, this approach enabled the identification of 23 proteins belonging to the Parkinson disease KEGG pathway, as well as proteins previously reported as PD circulating biomarkers. MDPI 2021-03-14 /pmc/articles/PMC7999506/ /pubmed/33799461 http://dx.doi.org/10.3390/ijms22062951 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Anastasi, Federica Masciandaro, Silvia Maria Carratore, Renata Del Dell’Anno, Maria Teresa Signore, Giovanni Falleni, Alessandra McDonnell, Liam A. Bongioanni, Paolo Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title | Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title_full | Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title_fullStr | Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title_full_unstemmed | Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title_short | Proteomics Profiling of Neuron-Derived Small Extracellular Vesicles from Human Plasma: Enabling Single-Subject Analysis |
title_sort | proteomics profiling of neuron-derived small extracellular vesicles from human plasma: enabling single-subject analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999506/ https://www.ncbi.nlm.nih.gov/pubmed/33799461 http://dx.doi.org/10.3390/ijms22062951 |
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