Department of Microbiology & Immunology, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
J Virol. 2012 Aug;86(16):8472-81. doi: 10.1128/JVI.05006-11. Epub 2012 May 30.
The HIV-1 capsid (CA) protein plays essential roles in both early and late stages of virl replication and has emerged as a novel drug target. We report hybrid structure-based virtual screening to identify small molecules with the potential to interact with the N-terminal domain (NTD) of HIV-1 CA and disrupt early, preintegration steps of the HIV-1 replication cycle. The small molecule 4,4'-[dibenzo[b,d]furan-2,8-diylbis(5-phenyl-1H-imidazole-4,2-diyl)]dibenzoic acid (CK026), which had anti-HIV-1 activity in single- and multiple-round infections but failed to inhibit viral replication in peripheral blood mononuclear cells (PBMCs), was identified. Three analogues of CK026 with reduced size and better drug-like properties were synthesized and assessed. Compound I-XW-053 (4-(4,5-diphenyl-1H-imidazol-2-yl)benzoic acid) retained all of the antiviral activity of the parental compound and inhibited the replication of a diverse panel of primary HIV-1 isolates in PBMCs, while displaying no appreciable cytotoxicity. This antiviral activity was specific to HIV-1, as I-XW-053 displayed no effect on the replication of SIV or against a panel of nonretroviruses. Direct interaction of I-XW-053 was quantified with wild-type and mutant CA protein using surface plasmon resonance and isothermal titration calorimetry. Mutation of Ile37 and Arg173, which are required for interaction with compound I-XW-053, crippled the virus at an early, preintegration step. Using quantitative PCR, we demonstrated that treatment with I-XW-053 inhibited HIV-1 reverse transcription in multiple cell types, indirectly pointing to dysfunction in the uncoating process. In summary, we have identified a CA-specific compound that targets and inhibits a novel region in the NTD-NTD interface, affects uncoating, and possesses broad-spectrum anti-HIV-1 activity.
HIV-1 衣壳 (CA) 蛋白在病毒复制的早期和晚期都发挥着重要作用,已成为新的药物靶点。我们报告了一种基于杂交结构的虚拟筛选方法,以鉴定具有与 HIV-1 CA 的 N 端结构域 (NTD) 相互作用并破坏 HIV-1 复制周期早期、整合前步骤的小分子的潜力。小分子 4,4'-[二苯并[b,d]呋喃-2,8-二基(5-苯基-1H-咪唑-4,2-二基)]二苯甲酸(CK026)在单次和多次感染中均具有抗 HIV-1 活性,但不能抑制外周血单核细胞(PBMC)中的病毒复制,因此被鉴定出来。合成并评估了 CK026 的三个类似物,它们的体积更小,具有更好的类药性。化合物 I-XW-053(4-(4,5-二苯基-1H-咪唑-2-基)苯甲酸)保留了母体化合物的所有抗病毒活性,并抑制了 PBMC 中多种原发性 HIV-1 分离株的复制,同时没有明显的细胞毒性。这种抗病毒活性是 HIV-1 特异性的,因为 I-XW-053 对 SIV 的复制或对一组非逆转录病毒没有影响。使用表面等离子体共振和等温滴定量热法定量测定了 I-XW-053 与野生型和突变 CA 蛋白的直接相互作用。Ile37 和 Arg173 的突变,这是与化合物 I-XW-053 相互作用所必需的,使病毒在早期、整合前阶段受损。使用定量 PCR,我们证明了 I-XW-053 的治疗抑制了多种细胞类型中的 HIV-1 逆转录,间接指向脱壳过程的功能障碍。总之,我们已经鉴定出一种 CA 特异性化合物,该化合物靶向并抑制 NTD-NTD 界面的新区域,影响脱壳,并具有广谱抗 HIV-1 活性。