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预测的猫冠状病毒刺突蛋白七肽重复 2 结构域的肽是有效的病毒感染抑制剂。

Peptides corresponding to the predicted heptad repeat 2 domain of the feline coronavirus spike protein are potent inhibitors of viral infection.

机构信息

Department of Nursing, Cardinal Tien Junior College of Healthcare and Management, New Taipei City, Taiwan.

出版信息

PLoS One. 2013 Dec 3;8(12):e82081. doi: 10.1371/journal.pone.0082081. eCollection 2013.

Abstract

BACKGROUND

Feline infectious peritonitis (FIP) is a lethal immune-mediated disease caused by feline coronavirus (FCoV). Currently, no therapy with proven efficacy is available. In searching for agents that may prove clinically effective against FCoV infection, five analogous overlapping peptides were designed and synthesized based on the putative heptad repeat 2 (HR2) sequence of the spike protein of FCoV, and the antiviral efficacy was evaluated.

METHODS

Plaque reduction assay and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) cytotoxicity assay were performed in this study. Peptides were selected using a plaque reduction assay to inhibit Feline coronavirus infection.

RESULTS

The results demonstrated that peptide (FP5) at concentrations below 20 μM inhibited viral replication by up to 97%. The peptide (FP5) exhibiting the most effective antiviral effect was further combined with a known anti-viral agent, human interferon-α (IFN-α), and a significant synergistic antiviral effect was observed.

CONCLUSION

Our data suggest that the synthetic peptide FP5 could serve as a valuable addition to the current FIP prevention methods.

摘要

背景

猫传染性腹膜炎(FIP)是一种由猫冠状病毒(FCoV)引起的致命免疫介导性疾病。目前,尚无疗效确切的治疗方法。在寻找可能对 FCoV 感染具有临床疗效的药物时,根据 FCoV 刺突蛋白的假定七肽重复 2(HR2)序列设计并合成了五个类似的重叠肽,并评估了其抗病毒功效。

方法

在这项研究中进行了噬斑减少测定和 MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)细胞毒性测定。使用噬斑减少测定法选择抑制猫冠状病毒感染的肽。

结果

结果表明,浓度低于 20 μM 的肽(FP5)可抑制病毒复制高达 97%。表现出最有效抗病毒作用的肽(FP5)进一步与已知的抗病毒药物人干扰素-α(IFN-α)联合使用,观察到显著的协同抗病毒作用。

结论

我们的数据表明,合成肽 FP5 可以作为当前 FIP 预防方法的有益补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ab/3849439/6b706119dd06/pone.0082081.g001.jpg

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