计算生物学
肽
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
传染性
2019年冠状病毒病(COVID-19)
生物
化学
病毒学
生物化学
病毒
医学
传染病(医学专业)
病理
疾病
作者
Danielle A. Guarracino,Jacqueline Iannaccone,Alexander Molina Cabrera,Sneha Kancharla
出处
期刊:ChemBioChem
[Wiley]
日期:2022-09-08
卷期号:23 (20)
被引量:3
标识
DOI:10.1002/cbic.202200415
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI