Protein Interactions Group, Center for Cancer Research Nanobiology Program, National Cancer Institute (NCI)-Frederick, National Institutes of Health (NIH), Frederick, MD 21702-1201, USA.
Antiviral Res. 2010 Oct;88(1):107-15. doi: 10.1016/j.antiviral.2010.08.004. Epub 2010 Aug 13.
Currently used antiretroviral therapy is highly successful but there is still a need for new effective and safe prophylactics and therapeutics. We have previously identified and characterized a human engineered antibody domain (eAd), m36, which exhibits potent broadly neutralizing activity against HIV-1 by targeting a highly conserved CD4 binding-induced (CD4i) structure on the viral envelope glycoprotein (Env) gp120. m36 has very small size (∼15kDa) but is highly specific and is likely to be safe in long-term use thus representing a novel class of potentially promising HIV-1 inhibitors. Major problems with the development of m36 as a candidate therapeutic are possible short serum half life and lack of effector functions that could be important for effective protection in vivo. Fusion of m36 to human IgG1 Fc resulted in dramatically diminished neutralization potency most likely due to the sterically restricted nature of the m36 epitope that limits access of large molecules. To confer effector functions and simultaneously increase the potency, we first matured m36 by panning and screening a mutant library for mutants with increased binding to gp120. We next fused m36 and its mutants with the first two domains (soluble CD4, sCD4) of the human CD4 using a polypeptide linker. Our results showed that the selected m36 mutants and the sCD4 fusion proteins exhibited more potent antiviral activities than m36. The m36-sCD4 fusion proteins with human IgG1 Fc showed even higher potency likely due to their bivalency and increased avidity although with a greater increase in molecular size. Our data suggest that m36 derivatives are promising HIV-1 candidate therapeutics and tools to study highly conserved gp120 structures with implications for understanding mechanisms of entry and design of vaccine immunogens and small-molecule inhibitors.
目前使用的抗逆转录病毒疗法非常成功,但仍需要新的有效和安全的预防和治疗方法。我们之前已经鉴定并表征了一种人类工程抗体结构域(eAd)m36,它通过靶向病毒包膜糖蛋白(Env)gp120 上高度保守的 CD4 结合诱导(CD4i)结构,表现出针对 HIV-1 的强大广谱中和活性。m36 具有非常小的尺寸(约 15kDa),但高度特异性,在长期使用中可能安全,因此代表了一类有前途的新型 HIV-1 抑制剂。将 m36 开发为候选治疗药物的主要问题可能是血清半衰期短,并且缺乏可能对体内有效保护很重要的效应功能。m36 与人 IgG1 Fc 的融合导致中和效力大大降低,这很可能是由于 m36 表位的空间限制性质限制了大分子的进入。为了赋予效应功能并同时提高效力,我们首先通过淘选和筛选突变文库来成熟 m36,以寻找与 gp120 结合增加的突变体。接下来,我们使用多肽接头将 m36 及其突变体与人类 CD4 的前两个结构域(可溶性 CD4,sCD4)融合。我们的结果表明,与 m36 相比,所选的 m36 突变体和 sCD4 融合蛋白表现出更强的抗病毒活性。m36-sCD4 融合蛋白与人 IgG1 Fc 显示出更高的效力,可能是由于它们的二价性和增加的亲和力,尽管分子尺寸增加更大。我们的数据表明,m36 衍生物是有前途的 HIV-1 候选治疗药物和工具,可用于研究高度保守的 gp120 结构,这对于理解进入机制、设计疫苗免疫原和小分子抑制剂具有重要意义。