Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid, Madrid, Spain.
PLoS One. 2011;6(9):e23877. doi: 10.1371/journal.pone.0023877. Epub 2011 Sep 8.
Virus capsid assembly constitutes an attractive target for the development of antiviral therapies; a few experimental inhibitors of this process for HIV-1 and other viruses have been identified by screening compounds or by selection from chemical libraries. As a different, novel approach we have undertaken the rational design of peptides that could act as competitive assembly inhibitors by mimicking capsid structural elements involved in intersubunit interfaces. Several discrete interfaces involved in formation of the mature HIV-1 capsid through polymerization of the capsid protein CA were targeted. We had previously designed a peptide, CAC1, that represents CA helix 9 (a major part of the dimerization interface) and binds the CA C-terminal domain in solution. Here we have mapped the binding site of CAC1, and shown that it substantially overlaps with the CA dimerization interface. We have also rationally modified CAC1 to increase its solubility and CA-binding affinity, and designed four additional peptides that represent CA helical segments involved in other CA interfaces. We found that peptides CAC1, its derivative CAC1M, and H8 (representing CA helix 8) were able to efficiently inhibit the in vitro assembly of the mature HIV-1 capsid. Cocktails of several peptides, including CAC1 or CAC1M plus H8 or CAI (a previously discovered inhibitor of CA polymerization), or CAC1M+H8+CAI, also abolished capsid assembly, even when every peptide was used at lower, sub-inhibitory doses. To provide a preliminary proof that these designed capsid assembly inhibitors could eventually serve as lead compounds for development of anti-HIV-1 agents, they were transported into cultured cells using a cell-penetrating peptide, and tested for antiviral activity. Peptide cocktails that drastically inhibited capsid assembly in vitro were also able to efficiently inhibit HIV-1 infection ex vivo. This study validates a novel, entirely rational approach for the design of capsid assembly interfacial inhibitors that show antiviral activity.
病毒衣壳组装构成了开发抗病毒疗法的有吸引力的靶标;已经通过筛选化合物或从化学文库中选择,鉴定出几种针对 HIV-1 和其他病毒的该过程的实验抑制剂。作为一种不同的、新颖的方法,我们已经着手设计可以通过模拟参与亚基界面的衣壳结构元件的肽,作为竞争性组装抑制剂。针对通过衣壳蛋白 CA 的聚合形成成熟 HIV-1 衣壳的几个离散界面进行了靶向研究。我们之前设计了一种肽 CAC1,它代表 CA 螺旋 9(二聚化界面的主要部分),并在溶液中结合 CA C 端结构域。在这里,我们已经确定了 CAC1 的结合位点,并表明它与 CA 二聚化界面基本重叠。我们还合理地修饰了 CAC1,以提高其溶解度和 CA 结合亲和力,并设计了另外四个代表参与其他 CA 界面的 CA 螺旋片段的肽。我们发现肽 CAC1、其衍生物 CAC1M 和 H8(代表 CA 螺旋 8)能够有效地抑制成熟 HIV-1 衣壳的体外组装。几种肽的鸡尾酒,包括 CAC1 或 CAC1M 加 H8 或 CAI(以前发现的 CA 聚合抑制剂),或 CAC1M+H8+CAI,也能消除衣壳组装,即使在每个肽以较低的亚抑制剂量使用时也是如此。为了提供这些设计的衣壳组装抑制剂最终可能作为开发抗 HIV-1 药物的先导化合物的初步证明,我们使用穿透细胞肽将它们输送到培养细胞中,并测试其抗病毒活性。在体外严重抑制衣壳组装的肽鸡尾酒也能够有效地抑制 HIV-1 感染。这项研究验证了一种设计衣壳组装界面抑制剂的新型、完全合理的方法,该方法显示出抗病毒活性。