Cell-Type-Specific CRISPR/Cas9 Delivery by Biomimetic Metal Organic Frameworks

被引:201
作者
Alyami, Mram Z. [1 ]
Alsaiari, Shahad K. [1 ]
Li, Yanyan [2 ]
Qutub, Somayah S. [1 ]
Aleisa, Fajr A. [2 ]
Sougrat, Rachid [3 ]
Merzaban, Jasmeen S. [2 ]
Khashab, Niveen M. [1 ]
机构
[1] KAUST, Adv Membranes & Porous Mat Ctr, Smart Hybrid Mat SHMs Lab, Thuwal 239556900, Saudi Arabia
[2] KAUST, Div Biol & Environm Sci Engn, Cell Migrat & Signaling Lab, Thuwal 239556900, Saudi Arabia
[3] KAUST, Adv Nanofabricat Imaging & Characterizat Ctr, Thuwal 239556900, Saudi Arabia
关键词
NANOPARTICLE DELIVERY; GENOME; CRISPR-CAS9; ACTIVATION; PROSPECTS;
D O I
10.1021/jacs.9b11638
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Effective and cell-type-specific delivery of CRISPR/Cas9 gene editing elements remains a challenging open problem. Here we report the development of biomimetic cancer cell coated zeolitic imidazolate frameworks (ZIFs) for targeted and cell-specific delivery of this genome editing machinery. Coating ZIF-8 that is encapsulating CRISPR/Cas9 (CC-ZIF) with a cancer cell membrane resulted in the uniformly covered C-3-ZIF((cell membrane type)). Incubation of C-3-ZIF(MCF) with MCF-7, HeLa, HDFn, and aTC cell lines showed the highest uptake by MCF-7 cells and negligible uptake by the healthy cells (i.e., HDFn and aTC). As to genome editing, a 3-fold repression in the EGFP expression was observed when MCF-7 were transfected with C-3-ZIF(MCF) compared to 1-fold repression in the EGFP expression when MCF-7 were transfected with C-3-ZIF(HELA). In vivo testing confirmed the selectivity of C-3-ZIF(MCF) to accumulate in MCF-7 tumor cells. This supports the ability of this biomimetic approach to match the needs of cell-specific targeting, which is unquestionably the most critical step in the future translation of genome editing technologies.
引用
收藏
页码:1715 / 1720
页数:6
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