The SARS-CoV-2, responsible for the COVID-19 pandemic, poses a significant threat to global healthcare. Peptide and peptide-based inhibitors, known for their safety, efficacy, and selectivity, have recently emerged as promising candidates for treating late-developing viral infections. In this study, three peptides were selected to target different stages of viral invasion, specifically ACE2 and S protein binding, as well as membrane fusion. The objective was to assess their ability to impede the entry of the SARS-CoV-2 Spike pseudotyped virus. Our findings revealed that a combination of these three peptides demonstrated enhanced antiviral effects. This outcome substantiates the feasibility of developing effective peptide combinations to combat diseases related to SARS-CoV-2. Moreover, the three-peptide combinations, designed to target multiple aspects of SARS-CoV-2 viral entry, exhibited heightened viral inhibition and broad-spectrum antiviral properties.
Synergistic peptide combinations designed to suppress SARS-CoV-2.
旨在抑制SARS-CoV-2的协同肽组合
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作者:Han Tao, Song Linhong, Niu Xinxin, Qiu Meng, Wang Yi, Wang Jing, Sun Xiuyan, Ma Jiali, Hu Siqi, Feng Zhichun
| 期刊: | Heliyon | 影响因子: | 3.600 |
| 时间: | 2024 | 起止号: | 2024 Apr 29; 10(9):e30489 |
| doi: | 10.1016/j.heliyon.2024.e30489 | 研究方向: | 信号转导 |
| 疾病类型: | 新冠 | ||
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