Department of Pharmacy, University of Napoli "Federico II", via D. Montesano 49, 80131 Napoli, Italy.
Dompé Farmaceutici SpA, via Campo di Pile, 67100 L'Aquila, Italy.
Int J Mol Sci. 2020 Aug 9;21(16):5707. doi: 10.3390/ijms21165707.
The pandemic evolution of SARS-CoV-2 infection is forcing the scientific community to unprecedented efforts to explore all possible approaches against COVID-19. In this context, targeting virus entry is a promising antiviral strategy for controlling viral infections. The main strategies pursued to inhibit the viral entry are considering both the virus and the host factors involved in the process. Primarily, direct-acting antivirals rely on inhibition of the interaction between ACE2 and the receptor binding domain (RBD) of the Spike (S) protein or targeting the more conserved heptad repeats (HRs), involved in the membrane fusion process. The inhibition of host TMPRSS2 and cathepsins B/L may represent a complementary strategy to be investigated. In this review, we discuss the development entry inhibitors targeting the S protein, as well as the most promising host targeting strategies involving TMPRSS2 and CatB/L, which have been exploited so far against CoVs and other related viruses.
SARS-CoV-2 感染的大流行演变迫使科学界以前所未有的努力探索对抗 COVID-19 的所有可能方法。在这种情况下,靶向病毒进入是一种有前途的抗病毒策略,可用于控制病毒感染。为了抑制病毒进入,主要采用了两种策略,既考虑了病毒本身,也考虑了参与该过程的宿主因素。直接作用的抗病毒药物主要依赖于抑制 ACE2 与 Spike(S)蛋白的受体结合域(RBD)之间的相互作用,或者靶向参与膜融合过程的更保守的七肽重复序列(HR)。抑制宿主 TMPRSS2 和组织蛋白酶 B/L 可能代表一种有待研究的互补策略。在这篇综述中,我们讨论了针对 S 蛋白的进入抑制剂的开发,以及迄今为止针对 CoV 和其他相关病毒的最有前途的宿主靶向策略,其中涉及 TMPRSS2 和 CatB/L。