首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >CRISPR/Cas9 Gene Editing to Make Conditional Mutants of Human Malaria Parasite P. falciparum
【2h】

CRISPR/Cas9 Gene Editing to Make Conditional Mutants of Human Malaria Parasite P. falciparum

机译:CRISPR / Cas9基因编辑使人类疟疾寄生虫恶性疟原虫有条件突变

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Malaria is a significant cause of morbidity and mortality worldwide. This disease, which primarily affects those living in tropical and subtropical regions, is caused by infection with Plasmodium parasites. The development of more effective drugs to combat malaria can be accelerated by improving our understanding of the biology of this complex parasite. Genetic manipulation of these parasites is key to understanding their biology; however, historically the genome of P. falciparum has been difficult to manipulate. Recently, CRISPR/Cas9 genome editing has been utilized in malaria parasites, allowing for easier protein tagging, generation of conditional protein knockdowns, and deletion of genes. CRISPR/Cas9 genome editing has proven to be a powerful tool for advancing the field of malaria research. Here, we describe a CRISPR/Cas9 method for generating glmS-based conditional knockdown mutants in P. falciparum. This method is highly adaptable to other types of genetic manipulations, including protein tagging and gene knockouts.
机译:疟疾是全世界发病和死亡的重要原因。该疾病主要影响生活在热带和亚热带地区的人们,是由疟原虫寄生虫感染引起的。通过提高我们对这种复杂寄生虫生物学的理解,可以加快开发更有效的药物来对抗疟疾。这些寄生虫的遗传操作是了解其生物学的关键。然而,从历史上看,恶性疟原虫的基因组一直难以操纵。最近,CRISPR / Cas9基因组编辑已用于疟疾寄生虫中,从而使蛋白质标签更容易,产生条件性蛋白质敲低和基因缺失。事实证明,CRISPR / Cas9基因组编辑是推进疟疾研究领域的强大工具。在这里,我们描述了一种用于在恶性疟原虫中生成基于glmS的条件敲除突变体的CRISPR / Cas9方法。该方法高度适用于其他类型的遗传操作,包括蛋白质标记和基因敲除。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号