bioRxiv : the preprint server for biology · 2026
Chemically modified CRISPR enzymes for multi-organ genome editing in vivo.
СтатьяПрепринтНазвание и аннотация: Перевод в очереди
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Baehr Christopher M, Ressnerova Alzbeta, Kang Min, Zhao Sheng, Le Beatrice, Haddad Rania F, Asija Kunica, Damante Mark, Sharma Rohit, George Christy, Huang Heidi, Assa Dror, Noel Eric A, Manohar Brigette, Otero P Anthony, Travis Meika, Saikaly Kayla, Hu Sophie, Van Laar Victor S, Lonser Russell R, Flannery John G, Murthy Niren, Wilson Ross C
Аннотация
Delivery remains the main obstacle to the development of in vivo genome editing therapies. CRISPR ribonucleoproteins confer high editing activity with transient exposure but lack intrinsic cell entry and targeting. Here we introduce PERCEPT, a delivery platform featuring reversible, covalent modification of CRISPR enzymes. PERCEPT enables modular installation of shielding polymers, amphiphilic delivery peptides and targeting ligands, allowing traceless cytosolic release of the native editor. A formulation incorporating an amphiphilic delivery peptide and the neuron-targeting ligand TET1 edited approximately 56% of striatal volume and 78% of neurons within edited regions after local striatal administration. In the R6/2 Huntington's disease model, PERCEPT mediated targeted editing of the mutant human HTT transgene, reducing mutant huntingtin aggregate burden and shifting local transcriptional programs away from inflammatory and injury-associated states. Tissue-adapted formulations edited 53% of Müller glia following intravitreal delivery, increased skeletal muscle reporter fluorescence tenfold versus unconjugated control following intramuscular injection, and enabled lung airway epithelial cell that persisted for three months following intranasal delivery. Rapid screening revealed that local anatomical and cellular barriers require distinct surface display for optimal editing. These results establish reversible chemical modification as a general strategy for adapting CRISPR enzyme delivery across multiple target tissues in vivo .