Understanding Intracellular Biology to Improve mRNA Delivery by Lipid Nanoparticles

Author:

Hunter Morag Rose1ORCID,Cui Lili1ORCID,Porebski Benjamin Thomas2ORCID,Pereira Sara1,Sonzini Silvia1ORCID,Odunze Uchechukwu1,Iyer Preeti3,Engkvist Ola3ORCID,Lloyd Rebecca Louise4,Peel Samantha4ORCID,Sabirsh Alan5ORCID,Ross‐Thriepland Douglas4,Jones Arwyn Tomos6ORCID,Desai Arpan Shailesh1

Affiliation:

1. Advanced Drug Delivery Pharmaceutical Sciences R&D, AstraZeneca Cambridge CB21 6GH UK

2. Protein and Nucleic Acid Chemistry MRC Laboratory of Molecular Biology Cambridge CB2 0QH UK

3. Molecular AI Discovery Sciences R&D, Astrazeneca Gothenburg 431 50 Sweden

4. Functional Genomics Discovery Sciences R&D, AstraZeneca Cambridge CB4 0WG UK

5. Advanced Drug Delivery Pharmaceutical Sciences R&D, AstraZeneca Gothenburg 431 50 Sweden

6. Cardiff School of Pharmacy and Pharmaceutical Sciences Cardiff University Cardiff CF10 3NB UK

Abstract

AbstractPoor understanding of intracellular delivery and targeting hinders development of nucleic acid‐based therapeutics transported by nanoparticles. Utilizing a siRNA‐targeting and small molecule profiling approach with advanced imaging and machine learning biological insights is generated into the mechanism of lipid nanoparticle (MC3‐LNP) delivery of mRNA. This workflow is termed Advanced Cellular and Endocytic profiling for Intracellular Delivery (ACE‐ID). A cell‐based imaging assay and perturbation of 178 targets relevant to intracellular trafficking is used to identify corresponding effects on functional mRNA delivery. Targets improving delivery are analyzed by extracting data‐rich phenotypic fingerprints from images using advanced image analysis algorithms. Machine learning is used to determine key features correlating with enhanced delivery, identifying fluid‐phase endocytosis as a productive cellular entry route. With this new knowledge, MC3‐LNP is re‐engineered to target macropinocytosis, and this significantly improves mRNA delivery in vitro and in vivo. The ACE‐ID approach can be broadly applicable for optimizing nanomedicine‐based intracellular delivery systems and has the potential to accelerate the development of delivery systems for nucleic acid‐based therapeutics.

Funder

AstraZeneca

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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