整合酶

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  • integrase;chelatase
整合酶整合酶
  1. 这是因为与蛋白酶和逆转录酶不同,整合酶在哺乳动物体内没有同源蛋白,因此有着更好的选择性。

    Different from protease and reverse transcriptase , the integrase has no counterpart in mammalian body , thus it has a better selectivity .

  2. HIV整合酶抑制剂体外筛选方法研究进展

    The Methods for Screening HIV Integrase Inhibitors in vitro

  3. 天然化合物抑制HIV整合酶的研究进展

    Advances in research of inhibiting HIV integral enzyme with natural compounds

  4. 在HIV的生命周期中,整合酶负责把病毒DNA整合到宿主细胞DNA中。

    In the life cycle of HIV , IN aids the integration of viral DNA into the host chromosome .

  5. 其中两种药物是“整合酶抑制剂”,它可以阻止艾滋病病毒的遗传物质附加到宿主细胞的DNA中。

    Two are " integrase inhibitors " that block the HIV genetic material from attaching to the host cell 's DNA .

  6. 用分子模拟方法研究HIV-1整合酶与抑制剂及病毒DNA的相互作用

    Study on the Interactions between HIV-1 Integrase with Inhibitors and Viral DNA with Molecular Simulation Approaches

  7. HIV-1整合酶(IN)通过依赖金属离子的两步反应将病毒DNA整合入宿主细胞中。

    HIV-1 integrase ( IN ) integrates viral DNA into host cells through two steps metal ions-dependent reactions .

  8. 化学生物学导向的HIV-1整合酶抑制剂的发现和结构优化

    Chemical Biology Directed Discovery and Structural Optimization of HIV-1 Integrase Inhibitors

  9. 基于结构的HIV-1整合酶抑制剂设计:计算机模拟方法

    Structure-Based Design of HIV-1 Integrase Inhibitors : A Computer Modeling Approach

  10. 多羟基芳香族化合物对HIV-1整合酶的抑制作用多羟基黄酮醇类化合物的合成

    Studies on the inhibition of polyhydroxylated aromatic compounds against HIV-1 integrase

  11. HIV-1整合酶四聚体结构模拟及其活性位点分析

    Modeling the Tetrameric Structure and Its Active Sites of HIV-1 Integrase

  12. HIV-1整合酶蛋白的可溶性表达及功能研究

    Prokaryotic Soluble Expression and Functional Study of HIV-1 Integrase Protein

  13. 用荧光方法检测HIV-1整合酶的体外活性

    Detection of HIV-1 Integrase in vitro Activities using Fluorescent Technology

  14. 它能够选择性地抑制HIV-1整合酶两个催化功能中的链转移过程。

    It can selectively inhibit strand transfer reaction of HIV-1 IN catalytic domain .

  15. 用分子对接方法预测HIV-1整合酶与金精三羧酸抑制剂的相互作用

    Prediction of the Interaction of HIV-1 Integrase and Inhibitor Aurintricarboxylic Acid Using Docking

  16. 乌药茎中鞣质类成分及其抗HIV-1整合酶活性研究

    Inhibitory activities of tannins extracted from stem of Lindera aggregata against HIV-1 integrase

  17. 用从头药物设计方法合理设计HIV-1整合酶抑制剂

    Rational design of HIV-1 integrase inhibitors using a de novo drug design method

  18. 人源抗HIV-1整合酶单链抗体基因的构建及表达

    Construction and expression of human anti HIV 1 integrase single chain antibody gene

  19. HIV-1整合酶全酶结构模拟及其抑制剂筛选

    The Structural Investigation of the HIV-1 Integrase Holoenzyme and the Screening of Its Inhibitors

  20. HIV-1整合酶的纯化及活性检测

    Purification and Assays for Activities of HIV-1 Integrase

  21. HIV-1整合酶与抑制剂金精三羧酸复合物的分子动力学模拟

    Molecular Dynamics Simulation on the Complex of HIV-1 Integrase and the Inhibitor Aurintricarboxylic Acid

  22. HIV-1整合酶酶联免疫吸附试验及其抑制剂的研究

    HIV-1 integrase enzymelinked immunosorbent assay and inhibitors

  23. HIV-1整合酶单链抗体对整合酶生物学活性抑制作用的研究

    Inhibition of enzymatic activities of HIV 1 integrase ( IN ) by the ScFv against IN

  24. 方法用I类整合酶基因通用引物对临床分离大肠埃希菌进行PCR检测,并对阳性菌株进行接合转移实验。

    Methods To detect the gene of class ⅰ integrase by PCR with universal primer and conjugal transfer the plasmid of class ⅰ integron positive strains .

  25. 因此,研究整合酶与DNA和抑制剂的相互作用机理对于抗HIV-1药物的设计和改造具有重要意义。

    Consequently , the study on the recognition mechanism of IN with inhibitors is important for the design and modification of the anti-HIV drugs .

  26. HIV-1整合酶抑制剂的研究进展

    Progress of HIV-1 Integrase Inhibitors

  27. 产生志贺样毒素的噬菌体φ297整合酶基因(int)的克隆和序列分析

    Cloning and Analysis of Integrase Gene ( int ) of Shiga Toxin-producing Bacteriophages φ 297

  28. 利用噬菌体表面呈现技术制备HIV-1整合酶单链抗体的初步研究

    A preliminary study on single chain fragments variable ( ScFv ) antibody against HIV 1 integrase by phage surface displaying

  29. 三联苯曲菌素还没有被广泛的研究但已报道显示其有抗氧化的活性,做为一种植物生长抑制剂,也显示了弱的抗HIV整合酶的活性。

    Terphenyllin has not been extensively studied but has been reported to exhibit anti-oxidative activity , acts as a plant growth inhibitor and shows weak activity against HIV integrase .

  30. 本论文的研究为先导化合物的优化打下了坚实的基础,推进了靶向HIV-1整合酶与LEDGF/p75相互作用界面的药物发现进程。

    This study laid a solid foundation for lead optimization and pushed forward the drug discovery process targeting IN-LEDGF / p75interaction .