HIV-1的核衣壳蛋白作为抗病毒药物的一个有前景的治疗靶点。

HIV therapy Pub Date : 2010-03-10 DOI:10.2217/HIV.10.3
V. Goldschmidt, L. Jenkins, H. Rocquigny, J. Darlix, Y. Mély
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引用次数: 33

摘要

核衣壳蛋白(NCp7)是一种主要的HIV-1结构蛋白,主要通过其保守的锌指指导与病毒核酸的特异性相互作用,在病毒复制中起关键作用。由于其高度保守性和关键功能,NCp7代表了可能补充HAART的药物的选择靶标,从而可能损害耐药HIV-1毒株的循环。锌喷射器显示出强大的抗逆转录病毒活性,但早期代遭受有限的选择性和显著的毒性。选择性提高的化合物已被开发出来,并正在探索作为局部杀菌剂的候选物。抑制NCp7与病毒核酸相互作用的几类分子也被开发出来。虽然小分子分子更适合用于药物开发,但通过筛选选择的大多数分子显示出有限的抗逆转录病毒活性。多肽和RNA适体似乎更有希望。
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The nucleocapsid protein of HIV-1 as a promising therapeutic target for antiviral drugs.
The nucleocapsid protein (NCp7) is a major HIV-1 structural protein that plays key roles in viral replication, mainly through its conserved zinc fingers that direct specific interactions with the viral nucleic acids. Owing to its high degree of conservation and critical functions, NCp7 represents a target of choice for drugs that can potentially complement HAART, thus possibly impairing the circulation of drug-resistant HIV-1 strains. Zinc ejectors showing potent antiretroviral activity were developed, but early generations suffered from limited selectively and significant toxicity. Compounds with improved selectivity have been developed and are being explored as topical microbicide candidates. Several classes of molecules inhibiting the interaction of NCp7 with the viral nucleic acids have also been developed. Although small molecules would be more suited for drug development, most molecules selected by screening showed limited antiretroviral activity. Peptides and RNA aptamers appear to be more promisin...
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