TY - JOUR
T1 - Snorkel-tag based affinity chromatography for recombinant extracellular vesicle purification
AU - Bobbili, Madhusudhan Reddy
AU - Görgens, André
AU - Yan, Yan
AU - Vogt, Stefan
AU - Gupta, Dhanu
AU - Corso, Giulia
AU - Barbaria, Samir
AU - Patrioli, Carolina
AU - Weilner, Sylvia
AU - Pultar, Marianne
AU - Jacak, Jaroslaw
AU - Hackl, Matthias
AU - Schosserer, Markus
AU - Grillari, Regina
AU - Kjems, Jørgen
AU - Andaloussi, Samir E.L.
AU - Grillari, Johannes
N1 - Publisher Copyright:
© 2024 The Author(s). Journal of Extracellular Vesicles published by Wiley Periodicals LLC on behalf of International Society for Extracellular Vesicles.
PY - 2024/10
Y1 - 2024/10
N2 - Extracellular vesicles (EVs) are lipid nanoparticles and play an important role in cell-cell communications, making them potential therapeutic agents and allowing to engineer for targeted drug delivery. The expanding applications of EVs in next generation medicine is still limited by existing tools for scaling standardized EV production, single EV tracing and analytics, and thus provide only a snapshot of tissue-specific EV cargo information. Here, we present the Snorkel-tag, for which we have genetically fused the EV surface marker protein CD81, to a series of tags with an additional transmembrane domain to be displayed on the EV surface, resembling a snorkel. This system enables the affinity purification of EVs from complex matrices in a non-destructive form while maintaining EV characteristics in terms of surface protein profiles, associated miRNA patterns and uptake into a model cell line. Therefore, we consider the Snorkel-tag to be a widely applicable tool in EV research, allowing for efficient preparation of EV standards and reference materials, or dissecting EVs with different surface markers when fusing to other tetraspanins in vitro or in vivo.
AB - Extracellular vesicles (EVs) are lipid nanoparticles and play an important role in cell-cell communications, making them potential therapeutic agents and allowing to engineer for targeted drug delivery. The expanding applications of EVs in next generation medicine is still limited by existing tools for scaling standardized EV production, single EV tracing and analytics, and thus provide only a snapshot of tissue-specific EV cargo information. Here, we present the Snorkel-tag, for which we have genetically fused the EV surface marker protein CD81, to a series of tags with an additional transmembrane domain to be displayed on the EV surface, resembling a snorkel. This system enables the affinity purification of EVs from complex matrices in a non-destructive form while maintaining EV characteristics in terms of surface protein profiles, associated miRNA patterns and uptake into a model cell line. Therefore, we consider the Snorkel-tag to be a widely applicable tool in EV research, allowing for efficient preparation of EV standards and reference materials, or dissecting EVs with different surface markers when fusing to other tetraspanins in vitro or in vivo.
KW - affinity chromatography
KW - CD81
KW - extracellular vesicles
KW - snorkel-tag
KW - StEVAC
KW - tetraspanins
KW - Humans
KW - MicroRNAs
KW - HEK293 Cells
KW - Chromatography, Affinity/methods
KW - Extracellular Vesicles/metabolism
KW - Tetraspanin 28/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85206280546&partnerID=8YFLogxK
U2 - 10.1002/jev2.12523
DO - 10.1002/jev2.12523
M3 - Article
C2 - 39400515
AN - SCOPUS:85206280546
SN - 2001-3078
VL - 13
SP - e12523
JO - Journal of Extracellular Vesicles
JF - Journal of Extracellular Vesicles
IS - 10
M1 - e12523
ER -