基因编码的基于双链DNA的纳米结构,由共价双价CRISPR/dCas系统折叠
Tiantian Wu1,2, Yuanwei Cao3,4, Qing Liu1
1CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190, China.
Journal of the American Chemical Society
|March 31, 2022
概括
研究人员开发了一种新的DNA纳米技术策略,使用聚类定期间隔的短平行列重复 (CRISPR) 和双链DNA. 这种方法为潜在的基因调节应用创造了新的混合纳米结构.
科学领域:
- 生物技术
- 纳米技术
- 分子生物学
背景情况:
- DNA纳米技术通常使用单链DNA杂交来构建纳米结构.
- 现有的方法在创建复杂,稳定的DNA纳米结构方面存在局限性.
研究的目的:
- 引入一种用于构建双链DNA-核蛋白 (RNP) 混合纳米结构的新策略.
- 使用共价双价集群定期间隔的简短的平行列重复 (CRISPR) /核酶死亡的CRISPR相关蛋白 (dCas) 系统进行DNA折叠.
主要方法:
- 通过响应刺激的链体的dCas9和dCas12a蛋白的融合产生双价RNP.
- 通过指导RNA激活RNP主,以准和绑定双链DNA支架上的特定序列.
- 通过RNP识别和结合诱导DNA折叠,形成混合纳米结构.
主要成果:
- 成功构建双链DNA-RNP混合纳米结构.
- 展示纳米结构在折叠状态下保护遗传信息的能力.
- 在纳米结构展开时呈现刺激响应基因转录.
结论:
- 通过使用基于CRISPR的RNP系统进行双链DNA折叠,开发的战略为DNA纳米技术提供了一种新方法.
- 这种方法为稳定的纳米结构形成和受控的基因调节提供了基因编码的平台.
- 这些发现为设计先进的功能性DNA纳米设备开辟了新的途径.
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