Affiliation:
1. Université Paris‐Saclay, INRAE, AgroParisTech Institut Jean‐Pierre Bourgin (IJPB), Versailles Versailles France
2. Core Biogenesis Illkirch Graffenstaden Versailles France
Abstract
AbstractPlants are gaining traction as a cost‐effective and scalable platform for producing recombinant proteins. However, expressing integral membrane proteins in plants is challenging due to their hydrophobic nature. In our study, we used transient and stable expression systems in Nicotiana benthamiana and Camelina sativa respectively to express SARS‐CoV‐2 E and M integral proteins, and target them to lipid droplets (LDs). LDs offer an ideal environment for folding hydrophobic proteins and aid in their purification through flotation. We tested various protein fusions with different linkers and tags and used 3D structure predictions to assess their effects. E and M mostly localized in the ER in Nicotiana benthamiana leaves but E could be targeted to LDs in oil accumulating tobacco when fused with oleosin, a LD integral protein. In Camelina sativa seeds, E and M were however found associated with purified LDs. By enhancing the accumulation of E and M within LDs through oleosin, we enriched these proteins in the purified floating fraction. This strategy provides an alternative approach for efficiently producing and purifying hydrophobic pharmaceuticals and vaccines using plant systems.This article is protected by copyright. All rights reserved
Subject
Molecular Medicine,Applied Microbiology and Biotechnology,General Medicine
Cited by
1 articles.
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