Brodsky A S, Erlacher H A, Williamson J R
MIT Department of Chemistry, Building 56-546, Cambridge, MA 02139, USA.
Nucleic Acids Res. 1998 Apr 15;26(8):1991-5. doi: 10.1093/nar/26.8.1991.
Formation of a specific complex between the HIV Tat protein and the small RNA element TAR is critical for activation of viral transcription. A model complex for this interaction composed of HIV-2 TAR and the amide derivative of arginine has been developed to study how Tat and TAR interact specifically. We have previously determined a high resolution NMR structure of the HIV-2 TAR-argininamide complex. The argininamide guanidium group hydrogen bonds to the major groove face of G26 and is stacked between U23 and A22, forming an arginine sandwich. This structure also provided evidence for formation of a U38-A27.U38 base triple, as U23 is positioned in the major groove within hydrogen bonding distance to A27. However, the expected U23 imino proton was not observed, preventing unambiguous identification of the base triple. Previous work on an isomorphic C38-G27.C23+ base triple mutant of the three base bulge HIV-1 TAR-argininamide complex demonstrated that the base triple is required for specific argininamide binding. Here we investigate the same C38-G27.C23+ base triple mutant in the context of two base bulge HIV-2 TAR. The improved NMR spectral properties of HIV-2 TAR allowed observation of the C23 amino and imino protons for the first time, providing direct evidence that a hydrogen bonding interaction is occurring. The NOEs observed correspond to those observed in the high resolution structure of the HIV-2 TAR-argininamide complex, confirming that a base triple is an important feature of the TAR-argininamide interaction.
HIV反式激活因子(Tat)蛋白与小RNA元件反式激活应答元件(TAR)之间形成特定复合物对于病毒转录激活至关重要。已构建了一个由HIV-2 TAR和精氨酸酰胺衍生物组成的该相互作用的模型复合物,以研究Tat与TAR如何特异性相互作用。我们之前已确定了HIV-2 TAR-精氨酸酰胺复合物的高分辨率核磁共振结构。精氨酸酰胺胍基与G26的大沟面形成氢键,并堆积在U23和A22之间,形成精氨酸三明治结构。该结构还为U38-A27.U38碱基三联体的形成提供了证据,因为U23位于与A27氢键距离内的大沟中。然而,未观察到预期的U23亚氨基质子,这妨碍了对碱基三联体的明确鉴定。先前对三碱基凸起HIV-1 TAR-精氨酸酰胺复合物的同构C38-G27.C23 +碱基三联体突变体的研究表明,该碱基三联体是精氨酸酰胺特异性结合所必需的。在此,我们在双碱基凸起HIV-2 TAR的背景下研究相同的C38-G27.C23 +碱基三联体突变体。HIV-2 TAR改善的核磁共振光谱特性首次允许观察到C23氨基和亚氨基质子,提供了氢键相互作用正在发生的直接证据。观察到的核Overhauser效应(NOE)与HIV-2 TAR-精氨酸酰胺复合物高分辨率结构中观察到的一致,证实碱基三联体是TAR-精氨酸酰胺相互作用的一个重要特征。