Giroud Charline, Du Yuhong, Marin Mariana, Min Qui, Jui Nathan T, Fu Haian, Melikyan Gregory B
1 Department of Pediatrics Infectious Diseases, Emory University School of Medicine , Atlanta, Georgia .
2 Department of Pharmacology, Emory University School of Medicine , Atlanta, Georgia .
Assay Drug Dev Technol. 2017 Feb/Mar;15(2):53-63. doi: 10.1089/adt.2017.777.
HIV-1 entry and fusion with target cells is an important target for antiviral therapy. However, a few currently approved treatments are not effective as monotherapy due to the emergence of drug resistance. This consideration has fueled efforts to develop new bioavailable inhibitors targeting different steps of the HIV-1 entry process. Here, a high-throughput screen was performed of a large library of 100,000 small molecules for HIV-1 entry/fusion inhibitors, using a direct virus-cell fusion assay in a 384 half-well format. Positive hits were validated using a panel of functional assays, including HIV-1 specificity, cytotoxicity, and single-cycle infectivity assays. One compound-4-(2,5-dimethyl-pyrrol-1-yl)-2-hydroxy-benzoic acid (DPHB)-that selectively inhibited HIV-1 fusion was further characterized. Functional experiments revealed that DPHB caused irreversible inactivation of HIV-1 Env on cell-free virions and that this effect was related to binding to the third variable loop (V3) of the gp120 subunit of HIV-1 Env. Moreover, DPHB selectively inhibited HIV-1 strains that use CXCR4 or both CXCR4 and CCR5 co-receptors for entry, but not strains exclusively using CCR5. This selectivity was mapped to the gp120 V3 loop using chimeric Env glycoproteins. However, it was found that pure DPHB was not active against HIV-1 and that its degradation products (most likely polyanions) were responsible for inhibition of viral fusion. These findings highlight the importance of post-screening validation of positive hits and are in line with previous reports of the broad antiviral activity of polyanions.
HIV-1进入靶细胞并与之融合是抗病毒治疗的一个重要靶点。然而,由于耐药性的出现,目前一些已获批的治疗方法作为单一疗法并不有效。这一考量推动了针对HIV-1进入过程不同步骤开发新型生物可利用抑制剂的努力。在此,使用384孔半孔板格式的直接病毒-细胞融合试验,对一个包含100,000个小分子的大型文库进行了高通量筛选,以寻找HIV-1进入/融合抑制剂。通过一系列功能试验对阳性命中物进行了验证,这些试验包括HIV-1特异性、细胞毒性和单周期感染性试验。对一种选择性抑制HIV-1融合的化合物——4-(2,5-二甲基-吡咯-1-基)-2-羟基苯甲酸(DPHB)——进行了进一步表征。功能实验表明,DPHB导致无细胞病毒粒子上的HIV-1 Env不可逆失活,且这种效应与结合HIV-1 Env的gp120亚基的第三个可变环(V3)有关。此外,DPHB选择性抑制使用CXCR4或同时使用CXCR4和CCR5共受体进入细胞的HIV-1毒株,但不抑制仅使用CCR5的毒株。利用嵌合Env糖蛋白将这种选择性定位到gp120 V3环上。然而,发现纯DPHB对HIV-1无活性,其降解产物(很可能是聚阴离子)负责抑制病毒融合。这些发现突出了对阳性命中物进行筛选后验证的重要性,并且与先前关于聚阴离子广泛抗病毒活性的报道一致。