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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...

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Autores principales: Anastasi, Federica, Masciandaro, Silvia Maria, Carratore, Renata Del, Dell’Anno, Maria Teresa, Signore, Giovanni, Falleni, Alessandra, McDonnell, Liam A., Bongioanni, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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