Li Taiming, Pan Junjie, Qi Jing, Zhang Chun
Sheng Wu Gong Cheng Xue Bao. 2015 Aug;31(8):1230-8.
AAV-ITR gene expression mini vector is a double-strand or single-strand DNA that only contains inverted terminal repeats of adeno-associated virus, cis-elements and gene of interest and does not contain any other foreign DNA sequences. We prepared Bac-ITR-EGFP and Bac-inrep. Spodoptera frugiperda cells were infected with Bac-ITR-EGFP (P3) and Bac-inrep (P3). Up to 100 μg of AAV-ITR-EGFP gene expression mini vectors were extracted from 2 x 10(7) cells of Sf9 72 h after infection. The gel electrophoresis analysis shows that most forms of AAV-ITR-EGFP gene expression mini vector were monomer and dimer. The mini vector expression efficacy was examined in vitro with HEK 293T cells. The EGFP expression was observed at 24 h after transfection, and the positive ratio reached 65% at 48 h after transfection.
腺相关病毒-反向末端重复序列(AAV-ITR)基因表达微型载体是一种双链或单链DNA,仅包含腺相关病毒的反向末端重复序列、顺式元件和目的基因,不包含任何其他外源DNA序列。我们制备了杆状病毒-ITR-增强绿色荧光蛋白(Bac-ITR-EGFP)和杆状病毒-inrep。用Bac-ITR-EGFP(P3)和Bac-inrep(P3)感染草地贪夜蛾细胞。感染后72小时,从2×10⁷个Sf9细胞中提取了多达100μg的AAV-ITR-EGFP基因表达微型载体。凝胶电泳分析表明,AAV-ITR-EGFP基因表达微型载体的大多数形式为单体和二聚体。用HEK 293T细胞在体外检测微型载体的表达效率。转染后24小时观察到增强绿色荧光蛋白(EGFP)表达,转染后48小时阳性率达到65%。