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)
|
PDF
Publisher pdf
Language: English
This work is licensed under a Creative Commons Attribution 4.0 International License.
|
|
|
Download this file (PDF/3MB) |
Preview |
| Request a format suitable for use with assistive technology e.g. a screenreader | |
|
PDF
Author's Accepted Manuscript
Language: English Restricted to Repository staff only |
|
|
Contact us about this publication
|
|
| Official URL: https://doi.org/10.1002/jev2.70354 |
|
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) |
- Link to SensusAccess
- Export to:
- RefWorks
- EPrints3 XML
- BibTeX
- CSV
- Depositors only (login required):

https://orcid.org/0000-0003-0190-8558
Altmetric
Altmetric