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Vesicle nucleation peptide fusion induced extracellular vesicles are distinct from Escherichia coli outer membrane vesicles, and provide an enhanced platform for protein production and purification

Streather, Bree, Eastwood, Tara, Baker, Karen, Liang, Mingzhi, Bailie, Alexandra, van der Velden, Tijn, Jeuken, Lars, Botchway, Stan W, Wang, Lin, Mulvihill, Daniel P. and others. (2026) Vesicle nucleation peptide fusion induced extracellular vesicles are distinct from Escherichia coli outer membrane vesicles, and provide an enhanced platform for protein production and purification. Journal of Extracellular Vesicles, 15 (8). Article Number e70354. ISSN 2001-3078. (In press) (doi:10.1002/jev2.70354) (KAR id:115793)

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Abstract

Bacterial outer membrane vesicles (OMVs), are nano-sized, spherical structures released by Gram-negative bacteria that play diverse roles in bacterial physiology, including communication, nutrient acquisition, and host interactions. These vesicles bud from the bacterial outer membrane and contain lipopolysaccharides, periplasmic proteins, nucleotides, and other biomolecules. The Vesicle Nucleating peptide (VNp) is a short peptide tag that, when fused to the amino terminus of a protein of interest, promotes the formation of bespoke recombinant extracellular vesicles (EVs) in Escherichia coli, enabling efficient production and simplified purification of recombinant proteins. Here, we characterise VNp-induced extracellular vesicles (VNp-EVs) and compare their composition and organisation with OMVs produced from E. coli expressing a periplasmic targeting fusion. While both vesicle types possess a single outer membrane-derived lipid bilayer, recombinant protein is highly enriched within the VNp-EVs compared to OMVs containing the periplasm targeting ssDsbA-fusion protein. VNp-fusions and the periplasm-targeted recombinant protein localize to distinct vesicle populations, with VNp-fusions showing markedly higher luminal concentrations and relative vesicular abundance, compared to the vesicles containing a periplasmic targeted fusion protein. OmpX co-expression further enriched the VNp-fusion content of vesicles, further enhancing yield. The VNp-vesicle lumen is an oxidizing environment, thus supports formation of inter- and intra-molecular disulfide bonds within encapsulated proteins. Overall, VNp-EVs represent a distinct class of recombinant extracellular vesicles that offer a simple and efficient route for producing and purifying concentrated, correctly folded recombinant proteins, expanding the utility of bacterial vesicle systems for biotechnological applications.

Item Type: Article
DOI/Identification number: 10.1002/jev2.70354
Uncontrolled keywords: biotechnology; downstream processing; extracellular vesicles; outer membrane vesicles; recombinant protein production
Subjects: Q Science > QH Natural history > QH581.2 Cell Biology
Q Science > QR Microbiology
Institutional Unit: Schools > School of Natural Sciences > Biosciences
Former Institutional Unit:
There are no former institutional units.
Funders: Biotechnology and Biological Sciences Research Council (https://ror.org/00cwqg982)
Depositing User: Daniel Mulvihill
Date Deposited: 26 Jul 2026 15:27 UTC
Last Modified: 28 Aug 2026 09:53 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/115793 (The current URI for this page, for reference purposes)

University of Kent Author Information

Streather, Bree.

Creator's ORCID: https://orcid.org/0000-0003-0190-8558
CReDIT Contributor Roles: Formal analysis, Data curation, Writing - review and editing, Investigation, Conceptualisation, Visualisation

Eastwood, Tara.

Creator's ORCID: https://orcid.org/0000-0003-2587-0574
CReDIT Contributor Roles: Writing - review and editing, Investigation

Baker, Karen.

Creator's ORCID: https://orcid.org/0000-0001-7628-1978
CReDIT Contributor Roles: Writing - review and editing, Investigation

Liang, Mingzhi.

Creator's ORCID: https://orcid.org/0000-0001-8925-6739
CReDIT Contributor Roles: Investigation

Mulvihill, Daniel P..

Creator's ORCID: https://orcid.org/0000-0003-2502-5274
CReDIT Contributor Roles: Conceptualisation, Resources, Funding acquisition, Data curation, Supervision, Writing - review and editing, Writing - original draft, Project administration
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