Engineered nucleocytosolic vehicles for loading of programmable editors

Julian Geilenkeuser(Helmholtz Zentrum München), Niklas Armbrust(Helmholtz Zentrum München), Emily Steinmaßl(Helmholtz Zentrum München), Samuel W. Du(University of California, Irvine), Sebastian Schmidt(Helmholtz Zentrum München), E. Binder(Helmholtz Zentrum München), Yuchun Li(Helmholtz Zentrum München), Niklas Wilhelm Warsing(Helmholtz Zentrum München), Stephanie Victoria Wendel(Helmholtz Zentrum München), F. Linde(Helmholtz Zentrum München), Elisa Marie Schiele(Helmholtz Zentrum München), Xiya Niu, Luisa Stroppel(Helmholtz Zentrum München), Oleksandr Berezin(Helmholtz Zentrum München), Tobias Heinrich Santl(Helmholtz Zentrum München), Tanja Orschmann(Helmholtz Zentrum München), Keith A. Nelson(Helmholtz Zentrum München), Christoph Gruber(Helmholtz Zentrum München), Grażyna Palczewska(University of California, Irvine), Carolline Rodrigues Menezes(University of California, Irvine), Eleonora Risaliti(University of California, Irvine), Zachary J Engfer(University of California, Irvine), Naile Koleci(TUM Klinikum), Andrea Schmidts(TUM Klinikum), Arie Geerlof(Helmholtz Zentrum München), Krzysztof Palczewski(University of California, Irvine), Gil G. Westmeyer(Helmholtz Zentrum München), Dong‐Jiunn Jeffery Truong(Helmholtz Zentrum München)
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Abstract

Advanced gene editing methods have accelerated biomedical discovery and hold great therapeutic promise, but safe and efficient delivery of gene editors remains challenging. In this study, we present a virus-like particle (VLP) system featuring nucleocytosolic shuttling vehicles that retrieve pre-assembled Cas-effectors via aptamer-tagged guide RNAs. This approach ensures preferential loading of fully assembled editor ribonucleoproteins (RNPs) and enhances the efficacy of prime editing, base editing, trans-activators, and nuclease activity coupled to homology-directed repair in multiple immortalized, primary, stem cell, and stem-cell-derived cell types. We also achieve additional protection of inherently unstable prime editing guide RNAs (pegRNAs) by shielding the 3'-exposed end with Csy4/Cas6f, further enhancing editing performance. Furthermore, we identify a minimal set of packaging and budding modules that can serve as a platform for bottom-up engineering of enveloped delivery vehicles. Notably, our system demonstrates superior per-VLP editing efficiency in primary T lymphocytes and two mouse models of inherited retinal disease, highlighting its therapeutic potential.


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