Influence of ionizable lipid tail length on lipid nanoparticle delivery of mRNA of varying length

Author:

Mrksich Kaitlin1,Padilla Marshall S.1,Joseph Ryann A.1,Han Emily L.1,Kim Dongyoon1,Palanki Rohan12,Xu Junchao1,Mitchell Michael J.13456ORCID

Affiliation:

1. Department of Bioengineering School of Engineering and Applied Science, University of Pennsylvania Philadelphia Pennsylvania USA

2. Center for Fetal Research Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

3. Abramson Cancer Center Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania USA

4. Center for Cellular Immunotherapies Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania USA

5. Penn Institute for RNA Innovation Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania USA

6. Institute for Immunology Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania USA

Abstract

AbstractRNA‐based therapeutics have gained traction for the prevention and treatment of a variety of diseases. However, their fragility and immunogenicity necessitate a drug carrier. Lipid nanoparticles (LNPs) have emerged as the predominant delivery vehicle for RNA therapeutics. An important component of LNPs is the ionizable lipid (IL), which is protonated in the acidic environment of the endosome, prompting cargo release into the cytosol. Currently, there is growing evidence that the structure of IL lipid tails significantly impacts the efficacy of LNP‐mediated mRNA translation. Here, we optimized IL tail length for LNP‐mediated delivery of three different mRNA cargos. Using C12‐200, a gold standard IL, as a model, we designed a library of ILs with varying tail lengths and evaluated their potency in vivo. We demonstrated that small changes in lipophilicity can drastically increase or decrease mRNA translation. We identified that LNPs formulated with firefly luciferase mRNA (1929 base pairs) and C10‐200, an IL with shorter tail lengths than C12‐200, enhance liver transfection by over 10‐fold. Furthermore, different IL tail lengths were found to be ideal for transfection of LNPs encapsulating mRNA cargos of varying sizes. LNPs formulated with erythropoietin (EPO), responsible for stimulating red blood cell production, mRNA (858 base pairs), and the C13‐200 IL led to EPO translation at levels similar to the C12‐200 LNP. The LNPs formulated with Cas9 mRNA (4521 base pairs) and the C9‐200 IL induced over three times the quantity of indels compared with the C12‐200 LNP. Our findings suggest that shorter IL tails may lead to higher transfection of LNPs encapsulating larger mRNAs, and that longer IL tails may be more efficacious for delivering smaller mRNA cargos. We envision that the results of this project can be utilized as future design criteria for the next generation of LNP delivery systems for RNA therapeutics.

Funder

National Institutes of Health

Canadian Aeronautics and Space Institute

American Cancer Society

National Institute of Dental and Craniofacial Research

National Science Foundation

Vagelos Institute for Energy Science and Technology, University of Pennsylvania

Publisher

Wiley

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