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HIV-1 逆转录酶 p51 亚单位的同源二聚化。

Homodimerization of the p51 subunit of HIV-1 reverse transcriptase.

机构信息

Laboratory of Structural Biology, MR-01, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.

出版信息

Biochemistry. 2010 Apr 6;49(13):2821-33. doi: 10.1021/bi902116z.

Abstract

The dimerization of HIV reverse transcriptase (RT), required to obtain the active form of the enzyme, is influenced by mutations, non-nucleoside reverse transcriptase inhibitors (NNRTIs), nucleotide substrates, Mg ions, temperature, and specifically designed dimerization inhibitors. In this study, we have utilized nuclear magnetic resonance (NMR) spectroscopy of the [methyl-(13)C]methionine-labeled enzyme and small-angle X-ray scattering (SAXS) to investigate how several of these factors influence the dimerization behavior of the p51 subunit. The (1)H-(13)C HSQC spectrum of p51 obtained at micromolar concentrations indicates that a significant fraction of the p51 adopts a "p66-like" conformation. SAXS data obtained for p51 samples were used to determine the fractions of monomer and dimer in the sample and to evaluate the conformation of the fingers/thumb subdomain. All of the p51 monomer observed was found to adopt the compact, "p51C" conformation observed for the p51 subunit in the RT heterodimer. The NMR and SAXS data indicate that the p51 homodimer adopts a structure that is similar to the p66/p51 heterodimer, with one p51C subunit and a second p51 subunit in an extended, "p51E" conformation that resembles the p66 subunit of the heterodimer. The fractional dimer concentration and the fingers/thumb orientation are found to depend strongly on the experimental conditions and exhibit a qualitative dependence on nevirapine and ionic strength (KCl) that is similar to the behavior reported for the heterodimer and the p66 homodimer. The L289K mutation interferes with p51 homodimer formation as it does with formation of the heterodimer, despite its location far from the dimer interface. This effect is readily interpreted in terms of a conformational selection model, in which p51(L289K) has a much greater preference for the compact, p51C conformation. A reduced level of dimer formation then results from the reduced ratio of the p51E(L289K) to p51C(L289K) monomers.

摘要

HIV 逆转录酶(RT)的二聚化是获得酶的活性形式所必需的,它受到突变、非核苷类逆转录酶抑制剂(NNRTIs)、核苷酸底物、Mg 离子、温度和专门设计的二聚化抑制剂的影响。在这项研究中,我们利用核磁共振(NMR)光谱学对 [甲基-(13)C]甲硫氨酸标记的酶和小角 X 射线散射(SAXS)的研究,探讨了这些因素如何影响 p51 亚基的二聚化行为。在微摩尔浓度下获得的 p51 的 (1)H-(13)C HSQC 谱表明,相当一部分 p51 采用了“p66 样”构象。为 p51 样品获得的 SAXS 数据用于确定样品中二聚体和单体的分数,并评估手指/拇指亚结构的构象。观察到的所有 p51 单体都被发现采用了在 RT 异二聚体中观察到的紧凑的“p51C”构象。NMR 和 SAXS 数据表明,p51 同源二聚体采用类似于 p66/p51 异二聚体的结构,一个 p51C 亚基和第二个 p51 亚基处于伸展的“p51E”构象中,类似于异二聚体的 p66 亚基。分数二聚体浓度和手指/拇指取向强烈依赖于实验条件,并表现出与报道的异二聚体和 p66 同源二聚体相似的依赖于奈韦拉平(nevirapine)和离子强度(KCl)的定性依赖性。L289K 突变干扰 p51 同源二聚体的形成,就像它干扰异二聚体的形成一样,尽管它位于远离二聚体界面的位置。这种效应很容易用构象选择模型来解释,其中 p51(L289K)对紧凑的 p51C 构象有更大的偏好。然后,由于 p51E(L289K)与 p51C(L289K)单体的比例降低,二聚体的形成水平降低。

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