Laboratory of Molecular Biophysics, MR-01, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709, USA.
Antiviral Res. 2009 Dec;84(3):205-14. doi: 10.1016/j.antiviral.2009.07.021. Epub 2009 Aug 7.
HIV reverse transcriptase (RT) is a primary target for drug intervention in the treatment of AIDS. We report the first solution NMR studies of [methyl-(13)C]methionine HIV-1 RT, aimed at better understanding the conformational and dynamic characteristics of RT, both in the presence and absence of the non-nucleoside RT inhibitor (NNRTI) nevirapine. The selection of methionine as a structural probe was based both on its favorable NMR characteristics, and on the presence of two important active site methionine residues, M184(66) and M230(66). Observation of the M184 resonance is subunit dependent; in the p66 subunit the solvent-exposed residue produces a readily observed signal with a characteristic resonance shift, while in the globular p51 subunit, the M184(51) resonance is shifted and broadened as M184 becomes buried in the protein interior. In contrast, although structural data indicates that the environment of M230 is also strongly subunit dependent, the M230 resonances from both subunits have very similar shift and relaxation characteristics. A comparison of chemical shift and intensity data with model-based predictions gives reasonable agreement for M184(66), while M230(66), located on the beta-hairpin "primer grip", is more mobile and solvent-exposed than suggested by crystal structures of the apo enzyme which have a "closed" fingers-thumb conformation. This mobility of the primer grip is presumably important for binding of non-nucleoside RT inhibitors (NNRTIs), since the NNRTI binding pocket is not observed in the absence of the inhibitors, requiring instead that the binding pocket be dynamically accessible. In the presence of the nevirapine, both the M184(66) and M230(66) resonances are significantly perturbed, while none of the methionine resonances in the p51 subunit is sensitive to this inhibitor. Site-directed mutagenesis indicates that both M16 and M357 produce two resonances in each subunit, and for both residues, the intensity ratio of the component peaks is strongly subunit dependent. Conformational features that might explain the multiple peaks are discussed.
HIV 逆转录酶(RT)是抗艾滋病药物干预的主要靶点。我们报告了首例 [甲基-(13)C]甲硫氨酸 HIV-1 RT 的溶液 NMR 研究,旨在更好地了解 RT 的构象和动态特性,包括有无非核苷类 RT 抑制剂(NNRTI)奈韦拉平的情况下。选择甲硫氨酸作为结构探针,既是基于其有利的 NMR 特性,也是基于两个重要的活性位点甲硫氨酸残基 M184(66)和 M230(66)的存在。M184 共振的观察取决于亚基;在 p66 亚基中,溶剂暴露的残基产生一个易于观察的信号,具有特征共振位移,而在球形的 p51 亚基中,M184(51)共振被位移和展宽,因为 M184 被埋藏在蛋白质内部。相比之下,尽管结构数据表明 M230 的环境也强烈依赖于亚基,但两个亚基的 M230 共振具有非常相似的位移和弛豫特征。化学位移和强度数据与基于模型的预测的比较对于 M184(66)给出了合理的一致性,而位于β发夹“引物夹”上的 M230(66)比apo 酶的晶体结构所表明的更为移动和溶剂暴露,apo 酶的晶体结构具有“闭合”的手指-拇指构象。这种引物夹的移动性对于非核苷类 RT 抑制剂(NNRTIs)的结合可能很重要,因为在没有抑制剂的情况下,NNRTI 结合口袋是观察不到的,因此需要该结合口袋具有动态可及性。在奈韦拉平存在的情况下,M184(66)和 M230(66)共振都受到显著干扰,而 p51 亚基中的任何甲硫氨酸共振都对这种抑制剂不敏感。定点突变表明,M16 和 M357 在每个亚基中都产生两个共振,对于这两个残基,峰的强度比强烈依赖于亚基。讨论了可能解释多峰的构象特征。