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A Mos1 transposase in vivo assay to screen new HIV-1 integrase inhibitors

机译:体内测定中的MOS1转座酶以筛选新的HIV-1整合酶抑制剂

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摘要

The integrase and transposase enzymes of retrovirus and transposons, respectively, share the catalytic DDE domain. In vitro assays showed that inhibitors of HIV-1 integrase generally inhibit the mariner Mos1 transposase. Using a Drosophila strain in which the mobilisation of the mariner element can be quantified by mosaic eyes, we showed that flies maintained in medium containing 210 A mu M to 4 mM of raltegravir, or 1 or 2 mM of dolutegravir, which are HIV-1 integrase inhibitor used in AIDS treatment, have 23-33% less somatic mobilisation in mosaic eyes when treated with raltegravir and 28-32% when treated with dolutegravir. The gene expression of the mariner transposase gene, estimated by qPCR, is similar among treated and control flies. The results suggest that in vivo assays using Drosophila can be used as a primary screening of inhibitory drugs for transposase and retroviral integrase. The advantages of this assay are that it is easy, quick, cheap and is an in vivo test, meaning that the tested substance has to have been taken in by cells and has arrived at the target site, which is not the case when in vitro assays are applied.
机译:分别是逆转录病毒和转座子的整体酶和转座酶,共用催化DDE结构域。体外测定表明,HIV-1整合酶的抑制剂通常抑制海里氏植物MOS1转座酶。使用果蝇元素的果酒菌株可以通过马赛克眼睛量化制冷菌菌株,我们表明,在含有210μm至4mm的Raltegravir或1或2mm的DoluteGravir中保持恒定的燃点,其是HIV-1当用roltegravir处理时,在艾滋病治疗中用于艾滋病治疗中的整体酶抑制剂在镶嵌时,在马赛克眼中具有23-33%的体细胞动员,而28-32%。通过QPCR估计的水手转座酶基因的基因表达在处理和对照苍蝇中类似。结果表明,使用果蝇的体内测定可以用作转座酶和逆转录病毒整合酶的抑制药物的主要筛选。该测定的优点是它很容易,快速,便宜,是体内测试,这意味着测试的物质必须通过细胞备份并达到靶位点,这不是体外时的情况应用测定。

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