RNA encoded peptide barcodes enable efficient in vivo screening of RNA delivery systems

Author:

Odunze Uchechukwu12ORCID,Rustogi Nitin3,Devine Paul3,Miller Lorraine4,Pereira Sara2,Vashist Surender1,Snijder Harm Jan5,Corkill Dominic6,Sabirsh Alan7,Douthwaite Julie1,Bond Nick3,Desai Arpan2

Affiliation:

1. Cell, Gene and RNA Therapy, Discovery Sciences, R&D, AstraZeneca , Cambridge , UK

2. Advanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca , Cambridge , UK

3. Physico-chemical Development, Biopharmaceuticals Development, R&D, AstraZeneca , Cambridge , UK

4. Animal Sciences and Technologies, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca , Cambridge , UK

5. Discovery Biology, Discovery Sciences, R&D, AstraZeneca , Gothenburg , Sweden

6. Bioscience in vivo, Early R&I, R&D, AstraZeneca , Cambridge , UK

7. Advanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca , Gothenburg , Sweden

Abstract

Abstract Lipid nanoparticles (LNPs) have been demonstrated to hold great promise for the clinical advancement of RNA therapeutics. Continued exploration of LNPs for application in new disease areas requires identification and optimization of leads in a high throughput way. Currently available high throughput in vivo screening platforms are well suited to screen for cellular uptake but less so for functional cargo delivery. We report on a platform which measures functional delivery of LNPs using unique peptide ‘barcodes’. We describe the design and selection of the peptide barcodes and the evaluation of these for the screening of LNPs. We show that proteomic analysis of peptide barcodes correlates with quantification and efficacy of barcoded reporter proteins both in vitro and in vivo and, that the ranking of selected LNPs using peptide barcodes in a pool correlates with ranking using alternative methods in groups of animals treated with individual LNPs. We show that this system is sensitive, selective, and capable of reducing the size of an in vivo study by screening up to 10 unique formulations in a single pool, thus accelerating the discovery of new technologies for mRNA delivery.

Funder

AstraZeneca R&D

AstraZeneca RNA Therapy

Publisher

Oxford University Press (OUP)

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