Peptide-guided lipid nanoparticles deliver mRNA to the neural retina of rodents and nonhuman primates

Author:

Herrera-Barrera Marco1ORCID,Ryals Renee C.23ORCID,Gautam Milan1ORCID,Jozic Antony1ORCID,Landry Madeleine1,Korzun Tetiana4ORCID,Gupta Mohit1,Acosta Chris1ORCID,Stoddard Jonathan3,Reynaga Rene3ORCID,Tschetter Wayne2ORCID,Jacomino Nick1,Taratula Oleh1ORCID,Sun Conroy1ORCID,Lauer Andreas K.2,Neuringer Martha23ORCID,Sahay Gaurav125ORCID

Affiliation:

1. Department of Pharmaceutical Sciences, College of Pharmacy, Robertson Life Sciences Building, Oregon State University, Portland, OR 97201, USA.

2. Department of Ophthalmology, Casey Eye Institute, Oregon Health and Science University, Portland, OR 97239, USA.

3. Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR 97006, USA.

4. Oregon Health and Science University Medical School, Portland, OR 97239, USA.

5. Department of Biomedical Engineering, Robertson Life Sciences Building, Oregon Health and Science University, Portland, OR 97201, USA.

Abstract

Lipid nanoparticle (LNP)–based mRNA delivery holds promise for the treatment of inherited retinal degenerations. Currently, LNP-mediated mRNA delivery is restricted to the retinal pigment epithelium (RPE) and Müller glia. LNPs must overcome ocular barriers to transfect neuronal cells critical for visual phototransduction, the photoreceptors (PRs). We used a combinatorial M13 bacteriophage–based heptameric peptide phage display library for the mining of peptide ligands that target PRs. We identified the most promising peptide candidates resulting from in vivo biopanning. Dye-conjugated peptides showed rapid localization to the PRs. LNPs decorated with the top-performing peptide ligands delivered mRNA to the PRs, RPE, and Müller glia in mice. This distribution translated to the nonhuman primate eye, wherein robust protein expression was observed in the PRs, Müller glia, and RPE. Overall, we have developed peptide-conjugated LNPs that can enable mRNA delivery to the neural retina, expanding the utility of LNP-mRNA therapies for inherited blindness.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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