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Novel insights into the isolation of extracellular vesicles by anion exchange chromatography

Koch, Leon F. ; Best, Tatjana ; Wüstenhagen, Elena ; Adrian, Klaus ; Rammo, Oliver ; Saul, Meike J. (2024)
Novel insights into the isolation of extracellular vesicles by anion exchange chromatography.
In: Frontiers in Bioengineering and Biotechnology, 2024, 11
doi: 10.26083/tuprints-00027155
Artikel, Zweitveröffentlichung, Verlagsversion

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Kurzbeschreibung (Abstract)

Extracellular vesicles (EVs) are membrane structures enclosed by a lipid bilayer that are released into the extracellular space by all types of cells. EVs are involved in many physiological processes by transporting biologically active substances. Interest in EVs for diagnostic biomarker research and therapeutic drug delivery applications has increased in recent years. The realization of the full therapeutic potential of EVs is currently hampered by the lack of a suitable technology for the isolation and purification of EVs for downstream pharmaceutical applications. Anion Exchange Chromatography (AEX) is an established method in which specific charges on the AEX matrix can exploit charges on the surface of EVs and their interactions to provide a productive and scalable separation and purification method. The established AEX method using Eshmuno® Q, a strong tentacle anion exchange resin, was used to demonstrate the principal feasibility of AEX-based isolation and gain insight into isolated EV properties. Using several EV analysis techniques to provide a more detailed insight into EV populations during AEX isolation, we demonstrated that although the composition of CD9/63/81 remained constant for tetraspanin positive EVs, the size distribution and purity changed during elution. Higher salt concentrations eluted larger tetraspanin negative vesicles.

Typ des Eintrags: Artikel
Erschienen: 2024
Autor(en): Koch, Leon F. ; Best, Tatjana ; Wüstenhagen, Elena ; Adrian, Klaus ; Rammo, Oliver ; Saul, Meike J.
Art des Eintrags: Zweitveröffentlichung
Titel: Novel insights into the isolation of extracellular vesicles by anion exchange chromatography
Sprache: Englisch
Publikationsjahr: 4 Juni 2024
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 19 Januar 2024
Ort der Erstveröffentlichung: Lausanne
Verlag: Frontiers Media S.A.
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Frontiers in Bioengineering and Biotechnology
Jahrgang/Volume einer Zeitschrift: 11
Kollation: 16 Seiten
DOI: 10.26083/tuprints-00027155
URL / URN: https://tuprints.ulb.tu-darmstadt.de/27155
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Herkunft: Zweitveröffentlichung DeepGreen
Kurzbeschreibung (Abstract):

Extracellular vesicles (EVs) are membrane structures enclosed by a lipid bilayer that are released into the extracellular space by all types of cells. EVs are involved in many physiological processes by transporting biologically active substances. Interest in EVs for diagnostic biomarker research and therapeutic drug delivery applications has increased in recent years. The realization of the full therapeutic potential of EVs is currently hampered by the lack of a suitable technology for the isolation and purification of EVs for downstream pharmaceutical applications. Anion Exchange Chromatography (AEX) is an established method in which specific charges on the AEX matrix can exploit charges on the surface of EVs and their interactions to provide a productive and scalable separation and purification method. The established AEX method using Eshmuno® Q, a strong tentacle anion exchange resin, was used to demonstrate the principal feasibility of AEX-based isolation and gain insight into isolated EV properties. Using several EV analysis techniques to provide a more detailed insight into EV populations during AEX isolation, we demonstrated that although the composition of CD9/63/81 remained constant for tetraspanin positive EVs, the size distribution and purity changed during elution. Higher salt concentrations eluted larger tetraspanin negative vesicles.

Freie Schlagworte: extracellular vesicles, ion-exchange chromatography, isolation, Eshmuno® Q, downstream processing, scalability, charge-based
ID-Nummer: Artikel-ID: 1298892
Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-271553
Zusätzliche Informationen:

This article is part of the Research Topic: Manufacturing of Next-Generation Biologics

Sec. Bioprocess Engineering

Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin, Gesundheit
Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie
10 Fachbereich Biologie > Extracellular vesicles / miRNA Research
Hinterlegungsdatum: 04 Jun 2024 12:48
Letzte Änderung: 05 Jun 2024 09:41
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