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用于设计抗人类尼帕病毒疫苗的CD8+免疫原性肽的鉴定

Identification of CD8+ Immunogenic Peptides for Vaccine Design against Nipah Virus in Humans.

作者信息

Suden Pankaj, Singh Inderpal, Chopra Chitrakshi, Mehta Malvika, Chandra Ratna, Bhushan Indu

机构信息

School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.

出版信息

Iran J Public Health. 2024 Dec;53(12):2789-2801.

Abstract

BACKGROUND

Nipah virus is a pathogenic virus of ruinous zoonotic potential with inflated rate of mortality in humans.

METHODS

Considering the emerging threat of this pandemic virus, the present investigation amid to design vaccine by using the bioinformatics tools such as host and virus codon usage analysis, CD8+ peptide prediction, immunogenicity/allergenicity/toxicity, MHC-I allele binding prediction and subsequent population coverage and MHC-I-peptide docking analysis.

RESULTS

In this study (conducted in 2022 at School of Biotechnology, Katra, India), a set of 11 peptides of the structural proteins of Nipah Virus were predicted and recognized by the set of MHC-I alleles that are expressed in 92% of the global human population.

CONCLUSION

The strong interactions between these peptides and the MHC-I protein suggest them as strong peptide candidates for the development of vaccine against Nipah Virus.

摘要

背景

尼帕病毒是一种具有毁灭性人畜共患病潜力的致病病毒,人类死亡率极高。

方法

鉴于这种大流行病毒带来的新威胁,本研究旨在利用生物信息学工具设计疫苗,如宿主和病毒密码子使用分析、CD8 + 肽预测、免疫原性/致敏性/毒性、MHC-I等位基因结合预测以及随后的群体覆盖率和MHC-I-肽对接分析。

结果

在本研究中(2022年于印度卡特拉生物技术学院进行),一组11种尼帕病毒结构蛋白的肽段被预测,并被在全球92%人口中表达的一组MHC-I等位基因识别。

结论

这些肽段与MHC-I蛋白之间的强相互作用表明它们是开发尼帕病毒疫苗的强有力候选肽段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e869/11693797/7278fe3eed82/IJPH-53-2789-g001.jpg

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