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Establishment of a well-characterized SARS-CoV-2 lentiviral pseudovirus neutralization assay using 293T cells with stable expression of ACE2 and TMPRSS2

机译:建立一种具有稳定表达ACE2和TMPRSS2的293T细胞的特征良好的SAR-COV-2慢病毒假豚藤病毒中和测定

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摘要

Pseudoviruses are useful surrogates for highly pathogenic viruses because of their safety, genetic stability, and scalability for screening assays. Many different pseudovirus platforms exist, each with different advantages and limitations. Here we report our efforts to optimize and characterize an HIV-based lentiviral pseudovirus assay for screening neutralizing antibodies for SARS-CoV-2 using a stable 293T cell line expressing human angiotensin converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2). We assessed different target cells, established conditions that generate readouts over at least a two-log range, and confirmed consistent neutralization titers over a range of pseudovirus input. Using reference sera and plasma panels, we evaluated assay precision and showed that our neutralization titers correlate well with results reported in other assays. Overall, our lentiviral assay is relatively simple, scalable, and suitable for a variety of SARS-CoV-2 entry and neutralization screening assays.
机译:由于其安全性,遗传稳定性和用于筛选测定的可扩展性,假纲病毒是具有高致病病毒的有用替代物。许多不同的Pseudovirus平台存在,每个平台都具有不同的优点和局限性。在这里,我们向我们的努力进行了优化和表征了一种基于HIV的慢病毒假缺鼠试验,用于使用表达人血管紧张素转换酶2(ACE2)和跨膜丝氨酸蛋白酶2(TMPRSS2)的稳定的293T细胞系来筛选SARS-COV-2的中和抗体。我们评估了不同的靶细胞,确定在至少两对数范围内产生读出的条件,并确认了一系列伪病毒输入中的一致中和滴度。使用参考血清和等离子体板,我们评估了测定精度,并显示了我们的中和滴度与其他测定中报道的结果相比好。总体而言,我们的慢病毒测定相对简单,可扩展,适用于各种SARS-COV-2进入和中和筛选测定。

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