蛋白水解靶向嵌合体多特异性抗病毒模式的分子设计与应用进展

Yang Zhou, Shujing Xu, Nerea López-Carrobles, Dang Ding, Xinyong Liu, L. Menéndez-Arias, P. Zhan
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引用次数: 1

摘要

病毒感染对人类健康和全球经济构成重大威胁;然而,目前大多数可用的抗病毒药物在限制病毒复制和选择耐药变异方面并不完全有效。靶向蛋白降解技术是避免或延缓耐药性出现的有前途的策略。在基于蛋白质降解的多特异性方法中,靶向嵌合体(proteolysis targeting chimera, PROTAC)是目前应用于抗病毒领域的主要策略。本文将介绍PROTAC技术的基本原理和作用机制,以及PROTAC相对于现有抗病毒药物的优势。我们还总结了PROTACs在抗病毒研究中的最新进展,讨论了存在的挑战,展望了未来抗病毒药物发现的机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent advances in the molecular design and applications of proteolysis targeting chimera-based multi-specific antiviral modality
Viral infections represent a major threat to human health and the global economy; however, most of the currently available antiviral drugs are not fully effective in restricting viral replication and selecting for drug-resistant variants. Targeted protein degradation technologies are promising strategies to avoid or delay the emergence of drug resistance. Among the protein degradation-based multi-specific approaches, proteolysis targeting chimera (PROTAC) is the main strategy applied in the antiviral field. In this review we will introduce the elements and mechanisms of action used by PROTAC technology, as well as the advantages of PROTACs over available antiviral drugs. We also summarize the latest progress in the application of PROTACs in antiviral research, discuss existing challenges and look into future opportunities for antiviral drug discovery.
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