Faculty of Pharmacy, Università degli Studi di Siena, Dipartimento Farmaco Chimico Tecnologico, Via Aldo Moro 2, 53100 Siena, Italy.
Curr Pharm Des. 2011 Nov;17(33):3713-28. doi: 10.2174/138161211798220972.
Protein-protein and protein-nucleic acid interactions are involved in many regulatory cellular pathways, playing a key role in cell growth and proliferation, as well as in the progression and development of various diseases such as infectious diseases. Especially in the anti-AIDS research, protein-protein and protein-nucleic acid complexes are being considered as promising targets for pharmaceutical interventions aimed at overcoming the drug resistance observed for most of the classic enzyme inhibitors. Consequently, more and more protein-protein and protein-nucleic acid interaction inhibitors have being identified and developed as candidate agents for antiretroviral therapy. Here, we review the state of the art in the discovery and development of protein-protein and protein-nucleic acid interaction inhibitors that block the main steps of the HIV-1 replication cycle, giving a medicinal chemistry-oriented view of strategies for inhibiting these regulatory interactions that are involved in the entry process, in the dimerization of reverse transcriptase and protease enzymes, and in the activity of the nucleocapsid protein by means of small molecular potential therapeutic agents.
蛋白质-蛋白质和蛋白质-核酸相互作用参与了许多调节细胞通路,在细胞生长和增殖中起着关键作用,并且在各种疾病(如传染病)的进展和发展中也起着关键作用。特别是在抗艾滋病研究中,蛋白质-蛋白质和蛋白质-核酸复合物被认为是药物干预的有前途的靶点,旨在克服大多数经典酶抑制剂的耐药性。因此,越来越多的蛋白质-蛋白质和蛋白质-核酸相互作用抑制剂被发现并开发为抗逆转录病毒治疗的候选药物。在这里,我们回顾了发现和开发蛋白质-蛋白质和蛋白质-核酸相互作用抑制剂的最新进展,这些抑制剂阻断了 HIV-1 复制周期的主要步骤,从药物化学的角度探讨了抑制这些调节相互作用的策略,这些调节相互作用涉及进入过程、逆转录酶和蛋白酶酶的二聚化以及核衣壳蛋白的活性,通过小分子潜在治疗剂。