Department of Bioengineering and Molecular Engineering and Sciences Institute, University of Washington, Seattle, WA 98195, United States; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, United States.
GenEdit Inc., Berkeley, CA, United States.
J Control Release. 2023 Feb;354:188-195. doi: 10.1016/j.jconrel.2022.12.057. Epub 2023 Jan 9.
Gene therapy approaches that utilize Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) ribonucleases have tremendous potential to treat human disease. However, CRISPR therapies delivered by integrating viral vectors are limited by potential off-target genome editing caused by constitutive activation of ribonuclease functions. Thus, biomaterial formulations are being used for the delivery of purified CRISPR components to increase the efficiency and safety of genome editing approaches. We previously demonstrated that a novel peptide identified by phage display, TAxI-peptide, mediates delivery of recombinant proteins into neurons. In this report we utilized NeutrAvidin protein to formulate neuron-targeted genome-editing nanoparticles. Cas12a ribonucleases was loaded with biotinylated guide RNA and biotinylated TAxI-peptide onto NeutrAvidin protein to coordinate the formation a targeted ribonuclease protein (RNP) complex. TAxI-RNP complexes are polydisperse with a 14.3 nm radius. The nanoparticles are stable after formulation and show good stability in the presence of normal mouse serum. TAxI-RNP nanoparticles increased neuronal delivery of Cas12a in reporter mice, resulting in induced tdTomato expression after direct injection into the dentate gyrus of the hippocampus. TAxI-RNP nanoparticles also increased genome editing efficacy in hippocampal neurons versus glia. These studies demonstrate the ability to assemble RNP nanoformulations with NeutrAvidin by binding biotinylated peptides and gRNA-loaded Cas12a ribonucleases into protein nanoparticles that target CRISPR delivery to specific cell-types in vivo. The potential to deliver CRISPR nanoparticles to specific cell-types and control off-target delivery to further reduce deleterious genome editing is essential for the creation of viable therapies to treat nervous system disease.
利用成簇规律间隔短回文重复序列 (CRISPR) 核糖核酸酶的基因治疗方法具有治疗人类疾病的巨大潜力。然而,通过整合病毒载体递送的 CRISPR 疗法受到核糖核酸酶功能组成性激活引起的潜在脱靶基因组编辑的限制。因此,正在使用生物材料制剂来递送纯化的 CRISPR 成分,以提高基因组编辑方法的效率和安全性。我们之前证明,噬菌体展示鉴定的新型肽 TAxI-肽介导重组蛋白递送至神经元。在本报告中,我们利用中性亲和素蛋白来配制靶向神经元的基因组编辑纳米颗粒。将 Cas12a 核糖核酸酶与生物素化向导 RNA 和生物素化 TAxI-肽加载到 NeutrAvidin 蛋白上,以协调靶向核糖核酸酶蛋白 (RNP) 复合物的形成。TAxI-RNP 复合物具有多分散性,半径为 14.3nm。纳米颗粒在制剂后稳定,并且在存在正常小鼠血清时表现出良好的稳定性。TAxI-RNP 纳米颗粒增加了 Cas12a 在报告小鼠中的神经元递送,导致直接注射到海马齿状回后诱导 tdTomato 表达。TAxI-RNP 纳米颗粒还增加了海马神经元与神经胶质细胞相比的基因组编辑效率。这些研究表明,通过将生物素化肽和负载 gRNA 的 Cas12a 核糖核酸酶结合到蛋白纳米颗粒中,能够将 RNP 纳米制剂与 NeutrAvidin 组装成体内靶向特定细胞类型的 CRISPR 递药,从而具有将 CRISPR 纳米颗粒递送至特定细胞类型并控制脱靶递药以进一步减少有害基因组编辑的潜力。这对于创建治疗神经系统疾病的可行疗法至关重要。