The effects of high shear rates on the average hydrodynamic diameter measured in biomimetic HIV Gag virus-like particle dispersions
- PMID: 38860137
- PMCID: PMC11163053
- DOI: 10.3389/fbioe.2024.1367405
The effects of high shear rates on the average hydrodynamic diameter measured in biomimetic HIV Gag virus-like particle dispersions
Abstract
HIV Gag virus-like particles (HIV Gag VLPs) are promising HIV vaccine candidates. In the literature, they are often described as shear-sensitive particles, and authors usually recommend the operation of tangential flow filtration (TFF) gently at shear rates below 4,000 s-1 to 6,000 s-1. This in turn poses a severe limitation to the performance of TFF-mediated concentration of VLPs, which would be substantially enhanced by working at higher shear rates. To our knowledge, studies examining the shear sensitivity of HIV Gag VLPs and providing detailed information and evidence for the fragility of these particles have not been conducted yet. Thus, we investigated the effect of high shear rates on the colloidal stability of mosaic VLPs (Mos-VLPs) as relevant examples for HIV Gag VLPs. For this purpose, Mos-VLPs were exposed to different shear rates ranging from 3,395 s-1 to 22, 365 s-1 for 2 h. The average hydrodynamic diameter (AHD) and the polydispersity index (PDI) of the associated particle size distribution were used as stability indicators and measured after the treatment and during storage through dynamic light scattering. At high shear rates, we observed an increase in both AHD and PDI during the storage of HIV Mos1.Gag VLPs (bVLP-without envelope proteins) and Mos1.Gag + Mos2S.Env VLPs (eVLP-with envelope proteins). eVLPs exhibited higher colloidal stability than bVLPs, and we discuss the potential stabilizing role of envelope proteins. We finally demonstrated that the dispersion medium also has a considerable impact on the stability of Mos-VLPs.
Keywords: HIV Gag virus-like particles; HIV vaccines; hydrodynamic diameter; mosaic virus-like particles; shear rate stability; shear-induced aggregation; virus-like particles.
Copyright © 2024 Wolf, Calisan, Stitz and Barbe.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
-
- Baden L. R., Stieh D. J., Sarnecki M., Walsh S. R., Tomaras G. D., Kublin J. G., et al. (2020). Safety and immunogenicity of two heterologous hiv vaccine regimens in healthy, hiv-uninfected adults (traverse): a randomised, parallel-group, placebo-controlled, double-blind, phase 1/2a study. lancet 7, e688–e698. 10.1016/S2352-3018(20)30229-0 - DOI - PMC - PubMed
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