Peptide Sequence of Pili Subunit Protein 49.8 kDa Shigella flexneri as Antigenic Epitope for Shigellosis Vaccine Development.

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Khoirul Anam, Agustina Tri Endharti, Sri Poeranto, Sumarno Reto Prawiro
{"title":"Peptide Sequence of Pili Subunit Protein 49.8 kDa <i>Shigella flexneri</i> as Antigenic Epitope for Shigellosis Vaccine Development.","authors":"Khoirul Anam,&nbsp;Agustina Tri Endharti,&nbsp;Sri Poeranto,&nbsp;Sumarno Reto Prawiro","doi":"10.4274/tjps.galenos.2021.75031","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This study investigates the amino acid sequence and identifies antigenic epitopes of 49.8 kilodalton (kDa) pili protein <i>Shigella flexner</i>i, which will be used as candidates for the shigellosis vaccine.</p><p><strong>Materials and methods: </strong>Our study is a prospectively descriptive laboratory. We used bacterial isolate of <i>S. flexneri</i> pili isolation was performed using a pili cutter and sodium dodecyl-sulfate polyacrylamide gel electrophoresis. The amino acid sequences were analyzed using liquid chromatography dual mass spectrometry (LC-MS/MS) method in the proteomic laboratory. The target epitope antigenicity analysis was tested using Kolaskar and Tongaonkar Antigenicity software. The Bepired Linear Epitope Prediction software is used for epitope mapping. PymOL software was used for the visualization of proteins and molecular docking. Peptides and antibodies were applied to hemagglutination test and immune response was tested using the dot blot method.</p><p><strong>Results: </strong>LC-MS/MS analysis results from the mascot server showed that the 49.8 kDa pili protein is <i>S. flexneri</i> similar to the flagellin protein of <i>S. flexneri</i> 1235-66 (ID I6H2T2). The results of antigenicity analysis and epitope mapping showed that areas of protein that has the most potential and antigenic epitopes are the regions 98-111 and 263-290 with the amino acid sequences, <i>QSSTGTNSQSDLDS</i> (Q-S) and <i>DTTITKAETKTVTKNQVVDTPVTTDAAK</i> (D-K). The results of the molecular docking interaction test between the peptide and the B-cell receptor have a low binding energy. Peptide Q-S and peptide D-K antigens are hemagglutinin molecules because they can agglutinate erythrocytes. The immune response between peptide antigens and anti-peptide antibodies can react based on color gradations in the dotblot method.</p><p><strong>Conclusion: </strong>The amino acid sequences Q-S and D-K are potentially antigenic epitopes. These peptides can be used to develop candidates for shigellosis vaccine.</p>","PeriodicalId":23378,"journal":{"name":"Turkish Journal of Pharmaceutical Sciences","volume":"19 6","pages":"649-656"},"PeriodicalIF":1.8000,"publicationDate":"2022-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780573/pdf/TJPS-19-649.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4274/tjps.galenos.2021.75031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: This study investigates the amino acid sequence and identifies antigenic epitopes of 49.8 kilodalton (kDa) pili protein Shigella flexneri, which will be used as candidates for the shigellosis vaccine.

Materials and methods: Our study is a prospectively descriptive laboratory. We used bacterial isolate of S. flexneri pili isolation was performed using a pili cutter and sodium dodecyl-sulfate polyacrylamide gel electrophoresis. The amino acid sequences were analyzed using liquid chromatography dual mass spectrometry (LC-MS/MS) method in the proteomic laboratory. The target epitope antigenicity analysis was tested using Kolaskar and Tongaonkar Antigenicity software. The Bepired Linear Epitope Prediction software is used for epitope mapping. PymOL software was used for the visualization of proteins and molecular docking. Peptides and antibodies were applied to hemagglutination test and immune response was tested using the dot blot method.

Results: LC-MS/MS analysis results from the mascot server showed that the 49.8 kDa pili protein is S. flexneri similar to the flagellin protein of S. flexneri 1235-66 (ID I6H2T2). The results of antigenicity analysis and epitope mapping showed that areas of protein that has the most potential and antigenic epitopes are the regions 98-111 and 263-290 with the amino acid sequences, QSSTGTNSQSDLDS (Q-S) and DTTITKAETKTVTKNQVVDTPVTTDAAK (D-K). The results of the molecular docking interaction test between the peptide and the B-cell receptor have a low binding energy. Peptide Q-S and peptide D-K antigens are hemagglutinin molecules because they can agglutinate erythrocytes. The immune response between peptide antigens and anti-peptide antibodies can react based on color gradations in the dotblot method.

Conclusion: The amino acid sequences Q-S and D-K are potentially antigenic epitopes. These peptides can be used to develop candidates for shigellosis vaccine.

志贺氏菌菌毛亚基蛋白49.8 kDa作为志贺氏菌疫苗抗原表位的肽序列
目的:研究49.8千道尔顿(kDa)佛氏志贺氏菌菌毛蛋白的氨基酸序列,并鉴定其抗原表位,为志贺氏菌病疫苗的候选物提供依据。材料和方法:我们的研究是前瞻性描述性实验室。本研究采用菌群分离法对flexneri菌毛进行分离,并用毛切割器和十二烷基硫酸钠聚丙烯酰胺凝胶电泳进行分离。氨基酸序列在蛋白质组学实验室采用液相色谱双质谱法(LC-MS/MS)进行分析。目的表位抗原性分析采用Kolaskar和Tongaonkar antigenicity软件进行。Bepired线性表位预测软件用于表位定位。使用PymOL软件对蛋白质进行可视化和分子对接。用多肽和抗体进行血凝试验,用点印迹法检测免疫应答。结果:从mascot server中提取的49.8 kDa菌毛蛋白与S. flexneri 1235-66 (ID I6H2T2)的鞭毛蛋白相似,为flexneri。抗原性分析和表位定位结果显示,氨基酸序列为QSSTGTNSQSDLDS (Q-S)和DTTITKAETKTVTKNQVVDTPVTTDAAK (D-K)的98-111和263-290的蛋白区最有潜力和抗原表位。肽与b细胞受体的分子对接相互作用试验结果显示其结合能较低。肽Q-S和肽D-K抗原是血凝素分子,因为它们能凝集红细胞。在斑点斑点法中,肽抗原和抗肽抗体之间的免疫反应可以根据颜色的渐变进行反应。结论:Q-S和D-K氨基酸序列是潜在的抗原表位。这些肽可用于开发志贺氏菌病候选疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.60
自引率
5.90%
发文量
79
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信