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Interactions of HIV-1 TAR RNA with Tat-derived peptides discriminated by on-line acoustic wave detector

机译:HIV-1 TAR RNA与在线声波检测器识别的Tat衍生肽的相互作用

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The human immunodeficiency virus type I is strongly regulated at the transcriptional level through the interaction of an 86-amino acid protein (Tat) with a viral messenger RNA transcript. Accordingly, the binding of this protein and other cellular factors to the RNA has constituted a significant target for the development of anti-HIV drugs. In the present work, we describe the detection of the binding of two Tat-derived peptides, of 12 and 40 amino acids in length, with chemically synthesized RNA by an acoustic wave sensor, Immobilization of the nucleic acid to the sensor surface, which was incorporated in an on-line system, was effected using the biotin-neutravidin interaction. As expected, the changes in series resonance frequency and motional resistance for the two peptides indicate reversible interactions in both cases that can be further characterized by the calculation of kinetic off-rates. Of particular interest is the nature of the two frequency-based signals, which are in opposite directions for the two peptides, These results together with those obtained for the surface interactions of neutravidin and biotinylated RNA confirm that the thickness shear mode sensor, mass-response model involving the well-known Sauerbrey expression is invalid when applied to operation in liquids. [References: 47]
机译:通过86个氨基酸的蛋白质(Tat)与病毒信使RNA转录物的相互作用,人类I型免疫缺陷病毒在转录水平受到了严格的调控。因此,该蛋白质和其他细胞因子与RNA的结合已成为开发抗HIV药物的重要目标。在当前的工作中,我们描述了通过声波传感器检测长度为12和40个氨基酸的两个Tat衍生肽与化学合成的RNA的结合,将核酸固定在传感器表面,这是利用生物素-中性亲和素相互作用来实现将其并入在线系统中。如预期的那样,两种肽的串联共振频率和运动阻力的变化表明在两种情况下都是可逆的相互作用,这可以通过动力学失速的计算来进一步表征。特别令人感兴趣的是两个基于频率的信号的性质,这两个信号的方向相反。这些结果以及中性亲和素和生物素化RNA的表面相互作用获得的结果证实了厚度剪切模式传感器的质量响应应用于著名的Sauerbrey表达式的模型在液体操作中无效。 [参考:47]

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