| Literature DB >> 29325201 |
Malthe Hansen-Bruhn1,2, Berta Esteban-Fernández de Ávila1, Mara Beltrán-Gastélum1, Jing Zhao1, Doris E Ramírez-Herrera1, Pavimol Angsantikul1, Kurt Vesterager Gothelf2, Liangfang Zhang1, Joseph Wang1.
Abstract
Direct and rapid intracellular delivery of a functional Cas9/sgRNA complex using ultrasound-powered nanomotors is reported. The Cas9/sgRNA complex is loaded onto the nanomotor surface through a reversible disulfide linkage. A 5 min ultrasound treatment enables the Cas9/sgRNA-loaded nanomotors to directly penetrate through the plasma membrane of GFP-expressing B16F10 cells. The Cas9/sgRNA is released inside the cells to achieve highly effective GFP gene knockout. The acoustic Cas9/sgRNA-loaded nanomotors display more than 80 % GFP knockout within 2 h of cell incubation compared to 30 % knockout using static nanowires. More impressively, the nanomotors enable highly efficient knockout with just 0.6 nm of the Cas9/sgRNA complex. This nanomotor-based intracellular delivery method thus offers an attractive route to overcome physiological barriers for intracellular delivery of functional proteins and RNAs, thus indicating considerable promise for highly efficient therapeutic applications.Entities:
Keywords: CRISPR/Cas9; GFP knockout; intracellular delivery; nanomotors; nanowires
Year: 2018 PMID: 29325201 DOI: 10.1002/anie.201713082
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336