相关实验视频
Updated: May 5, 2026

07:56
Genome Editing in Mammalian Cell Lines using CRISPR-Cas
Published on: April 11, 2019
21.5K
一个定制的酸协调器使CRISPR/Cas在现场放大
Tiantian Yang1,2, Man Tang1, Li Xu1
1The Center for Clinical Molecular Medical Detection, Innovative and Translational Laboratory of Molecular Diagnostics, Laboratory Medicine Center, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R.China.
Nucleic acids research
|March 3, 2026
概括
化学修饰的激活剂增强了CRISPR/Cas系统,用于敏感的分子诊断. 这种新的分散PS核酸驱动的Cas自催化系统 (SACA) 提高了灵敏度,并使得准确的现场成像.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 诊断 诊断 诊断 诊断
背景情况:
- 由于线性放大,CRISPR/Cas系统提供了强大的分子诊断,但对in situ成像的灵敏度有限.
- 酸 (PS) 改性核酸可以通过疏水性相互作用影响酶活性.
研究的目的:
- 设计一种新的CRISPR/Cas放大策略,以提高灵敏度和现场成像.
- 为了研究PS修饰在调节Cas酶活性中的机制.
- 开发一种用于精确分子诊断的新平台.
主要方法:
- 设计了带有"分散"PS修改的线性"协调器"探头.
- 开发了一个分散PS核酸驱动的Cas自催化系统 (SACA).
- 对Cas12a和Cas13a酶敏感性增强和细胞中HPVmRNA的现场成像进行了SACA测试.
主要成果:
- 在没有外部酶的情况下实现了指数放大,使Cas12a的灵敏度增加了5万倍,Cas13a的灵敏度增加了1万倍.
- 证明了线性探针的优越生物稳定性和结构简单性.
- 成功地在宫癌细胞中对HPV16和HPV18mRNA进行了精确的现场成像.
结论:
- 修改PS可以精确控制Cas酶激活和跨裂变抗性.
- SACA代表了高度敏感和高效的分子诊断的新范式.
- 这种方法促进了对Cas酶化学修饰核酸调节的理解.
相关概念视频
CRISPR
46.4K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
46.4K
Homologous Recombination
58.8K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
58.8K
Conservative Site-specific Recombination and Phase Variation
5.7K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
5.7K
CRISPR and crRNAs
14.6K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
14.6K
CRISPR/Cas9 Genome Editing
3.2K
The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
3.2K

