Influence of pH and lipid membrane on the liquid-liquid phase separation of wheat γ-gliadin in aqueous conditions

J Colloid Interface Sci. 2024 Aug 15:668:252-263. doi: 10.1016/j.jcis.2024.04.136. Epub 2024 Apr 24.

Abstract

Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used a microfluidic technique to encapsulate γ-gliadin within giant unilamellar vesicles (GUVs) and tune the physicochemical conditions in a controlled and rapid way. We examined the influence of pH and protein concentration on LLPS and protein-membrane interactions using various microscopy and spectroscopy techniques. We showed that γ-gliadin encapsulated in GUVs can undergo a pH-triggered liquid-liquid phase separation (LLPS) by two distinct mechanisms depending on the γ-gliadin concentration. At low protein concentrations, γ-gliadins phase separate by a nucleation and growth-like process, while, at higher protein concentration and pH above 6.0, γ-gliadin formed a bi-continuous phase suggesting a spinodal decomposition-like mechanism. Fluorescence and microscopy data suggested that γ-gliadin dense phase exhibited affinity for the GUV membrane, forming a layer at the interface and affecting the reversibility of the phase separation.

MeSH terms

  • Gliadin* / chemistry
  • Gliadin* / isolation & purification
  • Hydrogen-Ion Concentration
  • Membrane Lipids / chemistry
  • Phase Separation
  • Triticum* / chemistry
  • Unilamellar Liposomes* / chemistry
  • Unilamellar Liposomes* / metabolism
  • Water / chemistry

Substances

  • Gliadin
  • Unilamellar Liposomes
  • Water
  • Membrane Lipids