Endosomal Escape and Delivery of CRISPR/Cas9 Genome Editing Machinery Enabled by Nanoscale Zeolitic Imidazolate Framework

被引:439
作者
Alsaiari, Shahad K. [1 ]
Patil, Sachin [1 ]
Alyami, Mram [1 ]
Alamoudi, Kholod O. [1 ]
Aleisa, Fajr A. [2 ]
Merzaban, Jasmeen S. [2 ]
Li, Mo [3 ]
Khashab, Niveen M. [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Adv Membranes & Porous Mat Ctr, Smart Hybrid Mat SHMs Lab, Thuwal 239556900, Saudi Arabia
[2] King Abdullah Univ Sci & Technol KAUST, Div Biol & Environm Sci & Engn, Cell Migrat & Signaling Lab, Thuwal 239556900, Saudi Arabia
[3] King Abdullah Univ Sci & Technol KAUST, Div Biol & Environm Sci & Engn, Stem Cell & Regenerat Lab, Thuwal 239556900, Saudi Arabia
关键词
METAL-ORGANIC FRAMEWORKS; IN-VIVO; RNA; CHALLENGES; SYSTEM; CELLS; VITRO; CAS9;
D O I
10.1021/jacs.7b11754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CRISPR/Cas9 is a combined protein (Cas9) and an engineered single guide RNA (sgRNA) genome editing platform that offers revolutionary solutions to genetic diseases. It has, however, a double delivery problem owning to the large protein size and the highly charged RNA component. In this work, we report the first example of CRISPR/Cas9 encapsulated by nanoscale zeolitic imidazole frameworks (ZIFs) with a loading efficiency of 17% and enhanced endosomal escape promoted by the protonated imidazole moieties. The gene editing potential of CRISPR/Cas9 encapsulated by ZIF-8 (CC-ZIFs) is further verified by knocking down the gene expression of green fluorescent protein by 37% over 4 days. The nanoscale CC-ZIFs are biocompatible and easily scaled-up offering excellent loading capacity and controlled codelivery of intact Cas9 protein and sgRNA.
引用
收藏
页码:143 / 146
页数:4
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