Assessing Protein Corona Formation on Hard and Polymeric Nanoparticles – Towards Understanding Biocompatibility, Biodistribution, and Efficacy
ORAL · Invited
Abstract
Unpredictable protein adsorption on both hard and soft nanoparticles remains a considerable challenge towards effectively applying nanotechnologies in biological environments. Hard nanoparticles form the basis of many chemical nanosensors. Conversely, soft nanoparticles such as lipid nanoparticles (LNPs) are vital for the successful delivery of mRNA-based vaccines, and offer promising applications in immunotherapy and protein replacement therapy. Herein, we present a multimodal study of protein corona composition and dynamics, first on ‘hard’ nanoparticles: spherical polystyrene nanoparticles and high aspect ratio single-walled carbon nanotubes (SWCNTs). These nanoparticles are exposed to two biofluids of interest: blood plasma (relevant for intravenous applications) and cerebrospinal fluid (relevant for brain imaging and sensing applications). While polystyrene nanoparticles are relatively agnostic in the formation of their protein coronas, SWCNTs show strong preference for certain protein classes. Our analysis shows that corona compositions, and more broadly nanoparticle biofouling, can be drastically different for each nanoparticle type.
Next, we study nano-bio interactions encountered by ‘soft’ nanoparticles: LNPs commonly used for the therapeutic delivery of mRNA. We investigate how modifying (i) the mRNA packaged inside the LNPs and (ii) the ionizable lipid within the LNPs modulate the subsequently formed protein corona in (iii) various biological environments of relevance for delivery applications. Importantly, this workflow is readily translatable across soft polymer-based nanotechnologies of interest, which are understudied due to the experimental complexity of separating nanoparticle-corona complexes from free proteins. This fundamental understanding of protein-LNP interactions could enable more seamless design and clinical application of next-generation LNP carriers to bolster the safe and effective delivery of mRNA and other therapeutics to patients.
Next, we study nano-bio interactions encountered by ‘soft’ nanoparticles: LNPs commonly used for the therapeutic delivery of mRNA. We investigate how modifying (i) the mRNA packaged inside the LNPs and (ii) the ionizable lipid within the LNPs modulate the subsequently formed protein corona in (iii) various biological environments of relevance for delivery applications. Importantly, this workflow is readily translatable across soft polymer-based nanotechnologies of interest, which are understudied due to the experimental complexity of separating nanoparticle-corona complexes from free proteins. This fundamental understanding of protein-LNP interactions could enable more seamless design and clinical application of next-generation LNP carriers to bolster the safe and effective delivery of mRNA and other therapeutics to patients.
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Publication: Pinals, R.L., et al., Quantitative Protein Corona Composition and Dynamics on Carbon Nanotubes in Biological Environments. Angew Chem Int Ed Engl, 2020.doi:10.1101/2020.01.13.905356.<br><br>Pinals, R. L., Yang, D., Lui, A., Cao, W. & Landry, M. P. Corona Exchange Dynamics on Carbon Nanotubes by Multiplexed Fluorescence Monitoring. J. Am. Chem. Soc. 142, 1254–1264 (2020).
Presenters
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Markita P Landry
Chemical and Biomolecular Engineering, UC-Berkeley, University of California Berkeley
Authors
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Markita P Landry
Chemical and Biomolecular Engineering, UC-Berkeley, University of California Berkeley