在生物体内针对基因组编辑器的非病毒性输送
Connor A Tsuchida1,2, Kevin M Wasko2,3, Jennifer R Hamilton2,3
1University of California, Berkeley-University of California, San Francisco Graduate Program in Bioengineering, University of California, Berkeley, CA 94720.
概括
使用核糖核蛋白或mRNA进行基因组编辑传递的CRISPR-Cas的进步提供了短暂编辑器寿命和简化制造. 这些非病毒方法为生物发现提供了更有效和更容易获得的细胞和基因疗法.
科学领域:
- 分子生物学分子生物学
- 基因治疗 基因治疗
- 生物技术是生物技术.
背景情况:
- 细胞类型特定的基因组编辑工具在体内交付对于推动生物发现和细胞/基因疗法至关重要.
- 病毒载体在基因组编辑交付方面存在局限性,这促使需要替代策略.
研究的目的:
- 讨论最近在CRISPR-Cas基因组编辑分子的非病毒传递方面的进展.
- 突出核蛋白和mRNA输送系统的优点.
- 审查这些新兴交付方法的当前应用和未来机会.
主要方法:
- 关于CRISPR-Cas基因组编辑器的最新科学文献的审查.
- 专注于预组装的核糖蛋白复合体和mRNA编码的编辑器.
- 与病毒载体介导的传递方法进行比较.
主要成果:
- 通过核糖核蛋白或mRNA传递的CRISPR-Cas提供了暂时编辑器活性,减轻了与永久遗传修饰相关的风险.
- 这些非病毒策略避免了病毒载体的常见陷,例如免疫性和插入性突变发生.
- 精简的制造能力是一个关键优势,促进临床翻译和更广泛的可访问性.
结论:
- 新兴的CRISPR-Cas系统的非病毒传递方法准备彻底改变基因组编辑.
- 这些策略对未来的临床应用和更广泛的生物研究具有重大潜力.
相关概念视频
In-vitro Mutagenesis
13.9K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.9K
CRISPR
50.9K
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...
50.9K
Conservative Site-specific Recombination and Phase Variation
6.0K
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...
6.0K


