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NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform

机译:Nanobit System和Hydrofirimazine用于优化小鼠病毒感染的优化检测 - 一种小型成像平台

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摘要

Reporter genes are used to visualize intracellular biological phenomena, including viral infection. Here we demonstrate bioluminescent imaging of viral infection using the NanoBiT system in combination with intraperitoneal injection of a furimazine analogue, hydrofurimazine. This recently developed substrate has enhanced aqueous solubility allowing delivery of higher doses for in vivo imaging. The small high-affinity peptide tag (HiBiT), which is only 11 amino-acids in length, was engineered into a clinically used oncolytic adenovirus, and the complementary large protein (LgBiT) was constitutively expressed in tumor cells. Infection of the LgBiT expressing cells with the HiBiT oncolytic virus will reconstitute NanoLuc in the cytosol of the cell, providing strong bioluminescence upon treatment with substrate. This new bioluminescent system served as an early stage quantitative viral transduction reporter in vitro and also in vivo in mice, for longitudinal monitoring of oncolytic viral persistence in infected tumor cells. This platform provides novel opportunities for studying the biology of viruses in animal models.
机译:报告基因用于可视化细胞内生物现象,包括病毒感染。在这里,我们展示了使用纳米牛体系的病毒感染的生物发光成像,与腹腔内注射呋喃嗪类似物,氢纤维嗪。该最近开发的基材具有增强的含水溶解度,允许在体内成像中递送更高剂量。小型高亲和力肽标签(Hibit),其长度仅为11个氨基酸,被设计成临床用过的溶血性腺病毒,并且互补的大蛋白质(LGBit)在肿瘤细胞中形成。用HIBIT溶血性病毒感染LGBit表达细胞的细胞将在细胞的细胞溶胶中重组纳米,在用基材处理时提供强大的生物发光。这种新的生物发光系统作为早期定量病毒转导记者,并且在小鼠体内,用于纵向监测受感染的肿瘤细胞中的溶血性病毒持久性。该平台为研究动物模型中病毒生物学提供了新的机会。

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