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评估含有没食子酰基的儿茶素作为潜在 HIV-1 整合酶抑制剂。

The evaluation of catechins that contain a galloyl moiety as potential HIV-1 integrase inhibitors.

机构信息

Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, 28 Fu Xing Road, Hai Dian District, 100853 Beijing, China.

出版信息

Clin Immunol. 2010 Dec;137(3):347-56. doi: 10.1016/j.clim.2010.08.007. Epub 2010 Sep 15.

Abstract

Four catechins with the galloyl moiety, including catechin gallate (CG), epigallocatechin gallate (EGCG), gallocatechin gallate (GCG), and epicatechin gallate (ECG), were found to inhibit HIV-1 integrase effectively as determined by our ELISA method. In our docking study, it is proposed that when the HIV-1 integrase does not combine with virus DNA, the four catechins may bind to Tyr143 and Gln148, thus altering the flexibility of the loop (Gly140-Gly149), which could lead to an inhibition of HIV-1 integrase activity. In addition, after combining HIV-1 integrase with virus DNA, the four catechins may bind between the integrase and virus DNA, consequently, disrupt this interaction. Thus, the four catechins may reduce the activity of HIV-1 integrase by disrupting its interaction with virus DNA. The four catechins have a highly cooperative inhibitory effect (IC₅₀=0.1 μmol/L). Our study suggests that catechins with the galloyl moiety could be a novel and effective class of HIV-1 integrase inhibitors.

摘要

四种带有没食子酰基部分的儿茶素,包括没食子儿茶素(CG)、表没食子儿茶素没食子酸酯(EGCG)、没食子儿茶素没食子酸酯(GCG)和表儿茶素没食子酸酯(ECG),被发现通过我们的 ELISA 方法有效地抑制 HIV-1 整合酶。在我们的对接研究中,提出当 HIV-1 整合酶未与病毒 DNA 结合时,四种儿茶素可能与 Tyr143 和 Gln148 结合,从而改变环(Gly140-Gly149)的柔韧性,这可能导致 HIV-1 整合酶活性的抑制。此外,在 HIV-1 整合酶与病毒 DNA 结合后,四种儿茶素可能在整合酶和病毒 DNA 之间结合,从而破坏这种相互作用。因此,四种儿茶素可能通过破坏其与病毒 DNA 的相互作用来降低 HIV-1 整合酶的活性。四种儿茶素具有高度协同的抑制作用(IC₅₀=0.1 μmol/L)。我们的研究表明,带有没食子酰基部分的儿茶素可能是一类新型有效的 HIV-1 整合酶抑制剂。

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