University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093, USA.
Interdisciplinary Nanoscience Center (iNANO) and Department of Chemistry, Aarhus University, 8000, Aarhus C, Denmark.
Angew Chem Int Ed Engl. 2018 Mar 1;57(10):2657-2661. doi: 10.1002/anie.201713082. Epub 2018 Feb 6.
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.
本文报道了一种使用超声驱动的纳米马达将功能性 Cas9/sgRNA 复合物直接快速递送至细胞内的方法。Cas9/sgRNA 复合物通过可逆二硫键连接加载到纳米马达表面。5 分钟的超声处理可使负载 Cas9/sgRNA 的纳米马达直接穿透 GFP 表达的 B16F10 细胞的质膜。Cas9/sgRNA 在细胞内释放,实现 GFP 基因的高效敲除。与使用静态纳米线相比,在孵育细胞 2 小时内,声控 Cas9/sgRNA 负载的纳米马达使 GFP 敲除率超过 80%,而使用静态纳米线仅为 30%。更令人印象深刻的是,纳米马达仅使用 0.6nm 的 Cas9/sgRNA 复合物就能实现高效的敲除。因此,这种基于纳米马达的细胞内递药方法为克服功能性蛋白质和 RNA 细胞内递药的生理障碍提供了一种有吸引力的途径,从而为高效治疗应用提供了广阔的前景。