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Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation

Separation of highly enriched extracellular vesicles (EVs) fractions from milk is desirable for quantification, cargo analysis, functional characterization, and investigation as delivery vehicles for nutrients and/or therapeutics. However, a rigorous, reproducible protocol is lacking. This protocol...

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Detalles Bibliográficos
Autores principales: Mukhopadhya, Anindya, Santoro, Jessie, O’Driscoll, Lorraine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449126/
https://www.ncbi.nlm.nih.gov/pubmed/34568843
http://dx.doi.org/10.1016/j.xpro.2021.100821
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author Mukhopadhya, Anindya
Santoro, Jessie
O’Driscoll, Lorraine
author_facet Mukhopadhya, Anindya
Santoro, Jessie
O’Driscoll, Lorraine
author_sort Mukhopadhya, Anindya
collection PubMed
description Separation of highly enriched extracellular vesicles (EVs) fractions from milk is desirable for quantification, cargo analysis, functional characterization, and investigation as delivery vehicles for nutrients and/or therapeutics. However, a rigorous, reproducible protocol is lacking. This protocol considers a crucial aspect typically overlooked, i.e., that caseins are of similar size to, but more abundant than, EVs in milk. Our protocol combines acid pre-treatment and gradient ultracentrifugation, producing EV-enriched fractions suitable for downstream orthogonal characterization approaches. For complete details on the use and execution of this protocol, please refer to Mukhopadhya et al. (2021).
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spelling pubmed-84491262021-09-24 Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation Mukhopadhya, Anindya Santoro, Jessie O’Driscoll, Lorraine STAR Protoc Protocol Separation of highly enriched extracellular vesicles (EVs) fractions from milk is desirable for quantification, cargo analysis, functional characterization, and investigation as delivery vehicles for nutrients and/or therapeutics. However, a rigorous, reproducible protocol is lacking. This protocol considers a crucial aspect typically overlooked, i.e., that caseins are of similar size to, but more abundant than, EVs in milk. Our protocol combines acid pre-treatment and gradient ultracentrifugation, producing EV-enriched fractions suitable for downstream orthogonal characterization approaches. For complete details on the use and execution of this protocol, please refer to Mukhopadhya et al. (2021). Elsevier 2021-09-15 /pmc/articles/PMC8449126/ /pubmed/34568843 http://dx.doi.org/10.1016/j.xpro.2021.100821 Text en © 2021 The Author(s) https://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 Protocol
Mukhopadhya, Anindya
Santoro, Jessie
O’Driscoll, Lorraine
Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title_full Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title_fullStr Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title_full_unstemmed Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title_short Extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
title_sort extracellular vesicle separation from milk and infant milk formula using acid precipitation and ultracentrifugation
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449126/
https://www.ncbi.nlm.nih.gov/pubmed/34568843
http://dx.doi.org/10.1016/j.xpro.2021.100821
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