Engineered nucleocytosolic vehicles for loading of programmable editors

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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Publication Details

Journal
Cell
Published
2025-04-09
DOI
https://doi.org/10.1016/j.cell.2025.03.015
Citations
26
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
20.96
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article

Engineered nucleocytosolic vehicles for loading of programmable editors

Carolline Rodrigues Menezes, Andrea Schmidts, Tanja Orschmann, Egon Schiele et al.
26 citations
Cell
CRISPR and Genetic Engineering
20.96
article

Engineered nucleocytosolic vehicles for loading of programmable editors

Carolline Rodrigues Menezes, Andrea Schmidts, Tanja Orschmann, Egon Schiele, Samuel W. Du, Keith A. Nelson, E. Binder, Grażyna Palczewska, F. Linde, Gil G. Westmeyer, Tobias Heinrich Santl, Julian Geilenkeuser, Krzysztof Palczewski, Zachary J Engfer, Arie Geerlof, Dong‐Jiunn Jeffery Truong, Niklas Armbrust, Alexander Е. Berezin, Emily Steinmaßl, Stephanie Victoria Wendel, Christoph Gruber, Sebastian Schmidt, Yuchun Li, Luisa Stroppel, Niklas Wilhelm Warsing, Naile Koleci, Eleonora Risaliti, Xiya Niu
article en
26 citations

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.

CellVol. 188(10)
University of California, Irvine (US), TUM Klinikum (DE), Helmholtz Zentrum München (DE), Technical University of Munich (DE)
Openalex Percentile: Top 0%
CRISPR and Genetic Engineering
20.96
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