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Engineering a genetic construct to express soluble proteins tethered to the cell membrane

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Abstract

Synthetic biology has significantly grown and developed in the last decades, allowing its implementation in a wide variety of fields and applications. However, there is a lack of versatile, modular tools that allow the expression of soluble proteins anchored to the cell membrane, which could be useful in a range of applications. Therefore, using a combination of computational simulations and experimental validation, we designed a genetic construct for the expression of soluble proteins tethered to the cell membrane. Using green fluorescent protein as a model soluble protein, we demonstrated that it was successfully tethered to the cell membrane and that it could be incorporated into polymer lipid nanodiscs and purified through the histidine tag. Replacement of the reporter gene with another gene of interest could lead to its application in a wide variety of fields, from creating artificial signalling or enzymatic cascades to studying lipid and protein dynamics in the cell membrane.
Original languageEnglish
Article numberBSR20260216
Number of pages14
JournalBioscience Reports
Volume46
Issue number9
Early online date19 Aug 2026
DOIs
Publication statusPublished - 9 Sept 2026

Bibliographical note

Copyright © 2026 The Author(s). This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).

Data Access Statement

The underlying data for the present study can be found at the Aston Explorer Data Repository https://doi.org/10.17036/researchdata.aston.ac.uk.00000668

Funding

The authors are grateful for funding from the European Union’s Horizon 2020 research and innovation programme under Marie Sklodowska Curie [grant agreement No. 847,419 (MemTrain)]. The present work was also supported by the Aston University BBSRC Impact Accelerator Account [BB/X511031/1]. The Aston Institute for Membrane Excellence (AIME) is funded by UKRI’s Research England as part of their Expanding Excellence in England (E3) fund.

Keywords

  • GFP
  • membrane tethered protein
  • SMALP
  • WALP peptide

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