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利用抗病毒肽的治疗潜力和生物活性。

Harnessing the Therapeutic Potential and Biological Activity of Antiviral Peptides.

作者信息

Guarracino Danielle A, Iannaccone Jacqueline, Cabrera Alexander, Kancharla Sneha

机构信息

Department of Chemistry, The College of New Jersey, 2000 Pennington Rd., 08628, Ewing, NJ, USA.

出版信息

Chembiochem. 2022 Oct 19;23(20):e202200415. doi: 10.1002/cbic.202200415. Epub 2022 Sep 23.

Abstract

Peptides are ideal candidates for the development of antiviral therapeutics due to their specificity, chemical diversity and potential for highly potent, safe, molecular interventions. By restricting conformational freedom and flexibility, cyclic peptides frequently increase peptide stability. Viral targets are often very challenging as their evasive strategies for infectivity can preclude standard therapies. In recent years, several peptides from natural sources mitigated an array of viral infections. In parallel, short peptides derived from key viral proteins, modified with chemical groups such as lipids and cell-penetrating sequences, led to highly effective antiviral inhibitor designs. These strategies have been further developed during the recent COVID-19 pandemic caused by the novel coronavirus SARS-CoV-2. Several anti-SARS-CoV-2 peptides are gaining ground in pre-clinical development. Overall, peptides are strong contenders for lead compounds against many life-threatening viruses and may prove to be the key to future efforts revealing viral mechanisms of action and alleviating their effects.

摘要

由于其特异性、化学多样性以及进行高效、安全的分子干预的潜力,肽是开发抗病毒疗法的理想候选物。通过限制构象自由度和灵活性,环肽常常会提高肽的稳定性。病毒靶点往往极具挑战性,因为它们逃避感染的策略可能会使标准疗法失效。近年来,几种天然来源的肽减轻了一系列病毒感染。与此同时,源自关键病毒蛋白的短肽,用脂质和细胞穿透序列等化学基团进行修饰,产生了高效的抗病毒抑制剂设计。在由新型冠状病毒SARS-CoV-2引起的近期新冠疫情期间,这些策略得到了进一步发展。几种抗SARS-CoV-2肽在临床前开发中逐渐获得认可。总体而言,肽是对抗许多危及生命的病毒的先导化合物的有力竞争者,可能会成为未来揭示病毒作用机制并减轻其影响的关键。

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