University of Texas at El Paso, El Paso, TX, United States.
University of Texas at El Paso, El Paso, TX, United States; Laboratorio de Inmunología y Virología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, San Nicolas de los Garza, Mexico.
Adv Protein Chem Struct Biol. 2018;111:223-242. doi: 10.1016/bs.apcsb.2017.11.001. Epub 2017 Dec 18.
Viruses are obligate parasites that depend on cellular factors for replication. Pharmacological inhibition of essential viral proteins, mostly enzymes, is an effective therapeutic alternative in the absence of effective vaccines. However, this strategy commonly encounters drug resistance mechanisms that allow these pathogens to evade control. Due to the dependency on host factors for viral replication, pharmacological disruption of the host-pathogen protein-protein interactions (PPIs) is an important therapeutic alternative to block viral replication. In this review we discuss salient aspects of PPIs implicated in viral replication and advances in the development of small molecules that inhibit viral replication through antagonism of these interactions.
病毒是专性寄生生物,其复制依赖于细胞因子。在缺乏有效疫苗的情况下,抑制病毒必需蛋白(主要是酶)的药理作用是一种有效的治疗替代方法。然而,这种策略通常会遇到允许这些病原体逃避控制的耐药机制。由于病毒复制依赖于宿主因子,因此,通过阻断宿主-病原体蛋白-蛋白相互作用(PPIs)来破坏药物的药理作用是阻止病毒复制的重要治疗替代方法。在这篇综述中,我们讨论了参与病毒复制的 PPI 的显著方面,以及通过拮抗这些相互作用来开发抑制病毒复制的小分子的进展。