Bobyk Kostyantyn D, Mandadapu Sivakoteswara R, Lohith Katheryn, Guzzo Christina, Bhargava Abhishek, Lusso Paolo, Bewley Carole A
Laboratory of Bioorganic Chemistry, NIDDK, NIH , Bethesda, Maryland 20892, United States.
Laboratory of Immunoregulation, NIAID, NIH , Bethesda, Maryland 20892, United States.
Mol Pharm. 2017 Aug 7;14(8):2681-2689. doi: 10.1021/acs.molpharmaceut.7b00155. Epub 2017 Jul 13.
HIV/AIDS continues to pose an enormous burden on global health. Current HIV therapeutics include inhibitors that target the enzymes HIV protease, reverse transcriptase, and integrase, along with viral entry inhibitors that block the initial steps of HIV infection by preventing membrane fusion or virus-coreceptor interactions. With regard to the latter, peptides derived from the HIV coreceptor CCR5 were previously shown to modestly inhibit entry of CCR5-tropic HIV strains, with a peptide containing residues 178-191 of the second extracellular loop (peptide 2C) showing the strongest inhibition. Here we use an iterative approach of amino acid scanning at positions shown to be important for binding the HIV envelope, and recombining favorable substitutions to greatly improve the potency of 2C. The most potent candidate peptides gain neutralization breadth and inhibit CXCR4 and CXCR4/CCR5-using viruses, rather than CCR5-tropic strains only. We found that gains in potency in the absence of toxicity were highly dependent on amino acid position and residue type. Using virion capture assays we show that 2C and the new peptides inhibit capture of CD4-bound HIV-1 particles by antibodies whose epitopes are located in or around variable loop 3 (V3) on gp120. Analysis of antibody binding data indicates that interactions between CCR5 ECL2-derived peptides and gp120 are localized around the base and stem of V3 more than the tip. In the absence of a high-resolution structure of gp120 bound to coreceptor CCR5, these findings may facilitate structural studies of CCR5 surrogates, design of peptidomimetics with increased potency, or use as functional probes for further study of HIV-1 gp120-coreceptor interactions.
艾滋病毒/艾滋病继续给全球健康带来巨大负担。目前的抗艾滋病毒疗法包括针对艾滋病毒蛋白酶、逆转录酶和整合酶的抑制剂,以及通过阻止膜融合或病毒共受体相互作用来阻断艾滋病毒感染初始步骤的病毒进入抑制剂。关于后者,先前已表明源自艾滋病毒共受体CCR5的肽可适度抑制CCR5嗜性艾滋病毒株进入,其中包含第二个细胞外环(肽2C)178 - 191位残基的肽显示出最强抑制作用。在此,我们采用迭代方法,对显示对结合艾滋病毒包膜很重要的位置进行氨基酸扫描,并重组有利的取代以大幅提高2C的效力。最有效的候选肽获得了中和广度,可抑制使用CXCR4和CXCR4/CCR5的病毒,而不仅仅是CCR5嗜性毒株。我们发现,在无毒性情况下效力的提高高度依赖于氨基酸位置和残基类型。使用病毒体捕获试验,我们表明2C和新肽可抑制表位位于gp120可变环3(V3)或其周围的抗体捕获与CD4结合的HIV - 1颗粒。抗体结合数据分析表明,源自CCR5 ECL2的肽与gp120之间的相互作用更多地定位在V3的基部和茎部而非尖端周围。在缺乏与共受体CCR5结合的gp120高分辨率结构的情况下,这些发现可能有助于CCR5替代物的结构研究、设计效力增强的肽模拟物,或用作进一步研究HIV - 1 gp120 - 共受体相互作用的功能探针。