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Antiviral Potential of Catechins to Arrest Influenza Virus Infections with Confocal Microscopy, Molecular Docking and Mass Spectrometry

机译:儿茶素的抗病毒潜力抑制了共聚焦显微镜,分子对接和质谱法的流感病毒感染

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摘要

A combination of activity assays with confocal microscopy, sialidase inhibition assays, computer-based molecular docking and mass spectrometry show that catechins from tea leaves hold much promise as antiviral inhibitors to the influenza virus. Importantly they bind within the 430-cavity of influenza neuraminidase, remote from known drug resistant mutations, which render current antivirals ineffective.
机译:活性测定的组合与共聚焦显微镜,唾液酸酶抑制测定,计算机的分子对接和质谱表明,来自茶叶的儿茶素与流感病毒的抗病毒抑制剂保持了很大的承诺。重要的是,它们在流感神经氨酸酶的430腔内结合,远离已知的耐药突变,这使电流抗病毒无效。

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