Calcium Shock Enables Efficient and Programmable Particle Delivery for Genome Editing Applications
Classical intracellular delivery methods such as transfection and transduction are inefficient, particularly with confluent cells and organoids, and lack cell type-specific programmability. We demonstrate that an innovative methodology called calcium shock (CaSh) dramatically improves particle delivery into single cells, colonies, and organoids, and enables programmable delivery (CaSh-Pro) into specific cell types within heterocellular populations. Calcium shock works by increasing endocytotic uptake while simultaneously disarming cell-cell junctions. CaSh-Pro further incorporates specific molecular targeting agents and amphiphilic peptides for preferential editing of different cell types. Calcium shock improves expression of plasmid, ribonucleoprotein, or adeno-associated viral vectors with minimal toxicity in intact organoids representing diverse lineages. CaSh and CaSh-Pro provide simple, versatile protocols for genome editing in complex systems, to enable biological discovery and therapeutic development.
Authors
- Kunica Asija (ORCID: https://orcid.org/0000-0001-7272-0267)
- Dirk F. Hockemeyer (ORCID: https://orcid.org/0000-0002-5598-5092)
- Sophie M. Blackburn (ORCID: https://orcid.org/0000-0002-4197-0965)
- Nicole Vo
- Raymond J. Monnat (ORCID: https://orcid.org/0000-0001-7638-7393)
- Ross C. Wilson (ORCID: https://orcid.org/0000-0002-0644-5540)
- Lorena de Oñate
- Dana V. Foss (ORCID: https://orcid.org/0000-0003-2937-4703)
- Benjamin Freedman (ORCID: https://orcid.org/0000-0003-2228-7383)
- M. Frank (ORCID: https://orcid.org/0000-0002-4625-559X)
- Jasmine Villegas
- Hongxia Fu
- Xian Hu
Institutions
- QB3 (US)
- Northwest Kidney Centers (US)
- University of Oslo (NO)
- University of Washington (US)
- Innovative Genomics Institute (US)
- University of California, Berkeley (US)
Publication Details
- Journal
- Advanced Science
- Published
- 2026-03-17
- DOI
- https://doi.org/10.1002/advs.202510441
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00