Chepurna Oksana, Chatterjee Avradip, Li Yuanqing, Ding Hong, Murali Ramachandran, Black Keith L, Sun Tao
Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Department of Biomedical Sciences, Research Division of Immunology, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Polymers (Basel). 2025 Feb 5;17(3):417. doi: 10.3390/polym17030417.
Despite wide applications of CRISPR/Cas9 technology, effective approaches for CRISPR delivery with functional control are limited. In an attempt to develop a nanoscale CRSIPR/Cas9 delivery platform, we discovered that several biocompatible polymers, including polymalic acid (PMLA), polyglutamic acid (PGA), and polyaspartic acid (PLD), when conjugated with a trileucine (LLL) moiety, can effectively inhibit Cas9 nuclease function. The Cas9 inhibition by those polymers is dose-dependent, with varying efficiency to achieve 100% inhibition. Further biophysical studies revealed that PMLA-LLL directly binds the Cas9 protein, resulting in a substantial decrease in Cas9/sgRNA binding affinity. Transmission electron microscopy and molecular docking were performed to provide a possible binding mechanism for PMLA-LLL to interact with Cas9. This work identified a new class of Cas9 inhibitor in nano-polymer form. These biodegradable polymers may serve as novel Cas9 delivery vehicles with a potential to enhance the precision of Cas9-mediated gene editing.
尽管CRISPR/Cas9技术应用广泛,但实现具有功能控制的CRISPR递送的有效方法却很有限。为了开发一种纳米级CRSIPR/Cas9递送平台,我们发现几种生物相容性聚合物,包括聚苹果酸(PMLA)、聚谷氨酸(PGA)和聚天冬氨酸(PLD),当与三亮氨酸(LLL)部分共轭时,可以有效抑制Cas9核酸酶功能。这些聚合物对Cas9的抑制作用具有剂量依赖性,实现100%抑制的效率各不相同。进一步的生物物理研究表明,PMLA-LLL直接与Cas9蛋白结合,导致Cas9/sgRNA结合亲和力大幅下降。进行了透射电子显微镜和分子对接,以提供PMLA-LLL与Cas9相互作用的可能结合机制。这项工作鉴定出了一类新型的纳米聚合物形式的Cas9抑制剂。这些可生物降解的聚合物可能作为新型的Cas9递送载体,具有提高Cas9介导的基因编辑精度的潜力。