淘选
肽
视网膜
信使核糖核酸
噬菌体展示
细胞生物学
视网膜色素上皮
视网膜
肽库
生物
转染
体内
视觉光转导
分子生物学
神经科学
细胞培养
肽序列
生物化学
遗传学
基因
作者
Marco Herrera,Renee C. Ryals,Milan Gautam,Antony Jozić,Madeleine R. Landry,Tetiana Korzun,Mohit Gupta,Chris Acosta,Jonathan Stoddard,Rene Reynaga,Wayne W. Tschetter,Nick Jacomino,Oleh Taratula,Conroy Sun,Andreas Lauer,Martha Neuringer,Gaurav Sahay
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-01-11
卷期号:9 (2)
被引量:78
标识
DOI:10.1126/sciadv.add4623
摘要
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.
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