转染
绿色荧光蛋白
噬菌体
重组DNA
基因传递
噬菌体
衣壳
生物
分子生物学
报告基因
细胞
基因
转导(生物物理学)
病毒学
病毒
基因表达
大肠杆菌
遗传学
生物化学
作者
Farideh Ranjibar,Mahdi Habibi‐Anbouhi,Fatemeh Kazemi‐Lomedasht,Seyed Hamid Aghaee-Bakhtiyari,Ehsan Alirahimi,Mahdi Behdani
出处
期刊:DOAJ: Directory of Open Access Journals - DOAJ
日期:2018-09-01
卷期号:21 (9): 884-888
被引量:5
标识
DOI:10.22038/ijbms.2018.26191.6432
摘要
Filamentous bacteriophage M13 was genetically engineered to specifically target mammalian cells for gene delivery purpose.A vascular endothelial growth factor receptor 2 (VEGFR2)-specific nanobody was genetically fused to the capsid gene III of M13 bacteriophage (pHEN4/3VGR19). A mammalian expression construct containing Cop-green fluorescent protein (Cop-GFP), as a reporter gene, was amplified by PCR and then sub-cloned in the pHEN4/3VGR19 phagemid. The resulting construct was transfected into 293KDR cell. The recombinant phage was extracted and confirmed and then transduced into VEGFR2 expressing cell (293KDR).Seventy-two hr after transfection, green fluorescence was detected in 30% of the cells. About 1% of the cells which transduced by recombinant phages were able to express GFP.It is hoped that the results from this study will help to find potential vectors to improve the efficiency of gene delivery. Taken together, we conclude that this newly-introduced vector can be used in cancer researches.
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