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Detection of human immunodeficiency virus type 1 reverse transcriptase using aptamers as probes in affinity capillary electrophoresis

机译:使用适体作为亲和毛细管电泳中的探针检测人免疫缺陷病毒1型逆转录酶

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An affinity capillary electrophoresis/laser-induced fluorescence (CE/LIF) assay was developed for direct and specific detection of reverse transcriptase (RI) of the type I human immunodeficiency virus (HIV-1) using fluorescently labeled single-stranded DNA aptamers as probes. The aptamer used (Rr 26) is specific for HIV-1 RT, and it exhibited no cross-reactivity with RTs of the enhanced avian myeloblastosis virus (AMV), the Moloney murine leukemia virus (MMLV), or denatured HIV-1 RT An affinity complex of Rr 26-HIV-1 RT was readily formed, and calibration curves were linear up to 50 nM (6 mug/mL) HIV-1 RT concentration, with both the free probe and complex peak usable for analytical quantitation. Cell culture media (RPMI with 10% fetal bovine serum) interfered with the assay and aptamer-HIV-1 RT binding. Nonspecific binding was observed in low or undiluted culture, necessitating at least 100-fold dilution for analysis of raw culture samples.
机译:开发了一种亲和毛细管电泳/激光诱导的荧光(CE / LIF)分析法,用于使用荧光标记的单链DNA适体作为探针直接和特异性检测I型人类免疫缺陷病毒(HIV-1)的逆转录酶(RI) 。所使用的适体(Rr 26)对HIV-1 RT具有特异性,并且与增强的禽成纤维细胞病病毒(AMV),莫洛尼鼠白血病病毒(MMLV)或变性HIV-1 RT的RT没有交叉反应。 Rr 26-HIV-1 RT的亲和复合物很容易形成,并且校准曲线在高达50 nM(6马克/毫升)HIV-1 RT浓度下呈线性关系,游离探针和复合物峰均可用于分析定量。细胞培养基(含10%胎牛血清的RPMI)干扰了测定和适体-HIV-1 RT的结合。在低培养物或未稀释培养物中观察到非特异性结合,需要至少100倍稀释以分析生培养物样品。

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