Adeno-Associated Virus-like Particles' Response to pH Changes as Revealed by nES-DMA

Viruses. 2023 Jun 13;15(6):1361. doi: 10.3390/v15061361.

Abstract

Gas-phase electrophoresis on a nano-Electrospray Gas-phase Electrophoretic Mobility Molecular Analyzer (nES GEMMA) separates single-charged, native analytes according to the surface-dry particle size. A volatile electrolyte, often ammonium acetate, is a prerequisite for electrospraying. Over the years, nES GEMMA has demonstrated its unique capability to investigate (bio-)nanoparticle containing samples in respect to composition, analyte size, size distribution, and particle numbers. Virus-like particles (VLPs), being non-infectious vectors, are often employed for gene therapy applications. Focusing on adeno-associated virus 8 (AAV8) based VLPs, we investigated the response of these bionanoparticles to pH changes via nES GEMMA as ammonium acetate is known to exhibit these changes upon electrospraying. Indeed, slight yet significant differences in VLP diameters in relation to pH changes are found between empty and DNA-cargo-filled assemblies. Additionally, filled VLPs exhibit aggregation in dependence on the applied electrolyte's pH, as corroborated by atomic force microscopy. In contrast, cryogenic transmission electron microscopy did not relate to changes in the overall particle size but in the substantial particle's shape based on cargo conditions. Overall, we conclude that for VLP characterization, the pH of the applied electrolyte solution has to be closely monitored, as variations in pH might account for drastic changes in particles and VLP behavior. Likewise, extrapolation of VLP behavior from empty to filled particles has to be carried out with caution.

Keywords: AAV8; DMA; VLP; cryo-TEM; gene therapy; nES GEMMA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dependovirus* / genetics
  • Electrophoresis / methods
  • Hydrogen-Ion Concentration
  • Microscopy, Atomic Force

Substances

  • ammonium acetate

Grants and funding

This research was funded by Takeda and received financial support from TU Wien Bibliothek through its Open Access Funding programme. The Vienna BioCenter Core Facilities gratefully acknowledge funding from the Austrian Federal Ministry of Education, Science and Research and the city of Vienna.