贾第鞭毛虫α -8贾第丁免疫优势抗原表位的抗原鉴定

Chao-jun Wei, Yan-juan Jia, Hui Xu, Ling Wu, Si-qi Lu, Yong-hong Li
{"title":"贾第鞭毛虫α -8贾第丁免疫优势抗原表位的抗原鉴定","authors":"Chao-jun Wei,&nbsp;Yan-juan Jia,&nbsp;Hui Xu,&nbsp;Ling Wu,&nbsp;Si-qi Lu,&nbsp;Yong-hong Li","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To identify the dominant epitopes of α-8 giardin in Giardia lamblia, and analyze their immunoreactivity.</p><p><strong>Methods: </strong>Three dominant epitopes G1(7-17 aa), G2(30-40 aa) and G3(296-306 aa) were predicted for α-8 giardin by bioinformatic analysis using DNAstar, Biosun and CLUSTAL W softwares. Each epitope was conjugated to keyhole limpethemocyanin (KLH) and then used to immunize female Chinchilla rabbits via multi-point(8-10 points) subcutaneous injections on the back(0.5 mg conjugate/rabbit, 100 μl at each point). Then the rabbits were boosted(0.2 mg conjugate/rabbit) on days 14, 21 and 28 after the first immunization. Blood was collected prior to each immunization, and carotid artery blood(50 ml) was collected on day 7 after the last immunization. The antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was determined with indirect ELISA. The reactivity of the three anti-sera with recominant giardin (rGiardin) was analyzed with Western blotting.</p><p><strong>Results: </strong>The concentration of the purified conjugates KLH-G1, KLH-G2, and KLH-G3 was 0.66, 0.95 and 0.25 mg/ml, respectively. ELISA showed that the antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was 1∶12800, 1∶51200, 1∶51200, respectively. SDS-PAGE revealed a specific band at M(r) 36 000 for the three anti-sera. Western blotting showed that the three anti-sera all specifically recognized rGiardin.</p><p><strong>Conclusion: </strong>Immunization with the KLH-G1, KLH-G2, and KLH-G3 conjugates induced production of specific IgG antibody in rabbits, which can recognize rGiardin.</p>","PeriodicalId":23981,"journal":{"name":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","volume":"34 5","pages":"389-93"},"PeriodicalIF":0.0000,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Antigenic Characterization of Immunodominant Epitopes of Alpha-8 giardin in Giardia lamblia].\",\"authors\":\"Chao-jun Wei,&nbsp;Yan-juan Jia,&nbsp;Hui Xu,&nbsp;Ling Wu,&nbsp;Si-qi Lu,&nbsp;Yong-hong Li\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To identify the dominant epitopes of α-8 giardin in Giardia lamblia, and analyze their immunoreactivity.</p><p><strong>Methods: </strong>Three dominant epitopes G1(7-17 aa), G2(30-40 aa) and G3(296-306 aa) were predicted for α-8 giardin by bioinformatic analysis using DNAstar, Biosun and CLUSTAL W softwares. Each epitope was conjugated to keyhole limpethemocyanin (KLH) and then used to immunize female Chinchilla rabbits via multi-point(8-10 points) subcutaneous injections on the back(0.5 mg conjugate/rabbit, 100 μl at each point). Then the rabbits were boosted(0.2 mg conjugate/rabbit) on days 14, 21 and 28 after the first immunization. Blood was collected prior to each immunization, and carotid artery blood(50 ml) was collected on day 7 after the last immunization. The antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was determined with indirect ELISA. The reactivity of the three anti-sera with recominant giardin (rGiardin) was analyzed with Western blotting.</p><p><strong>Results: </strong>The concentration of the purified conjugates KLH-G1, KLH-G2, and KLH-G3 was 0.66, 0.95 and 0.25 mg/ml, respectively. ELISA showed that the antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was 1∶12800, 1∶51200, 1∶51200, respectively. SDS-PAGE revealed a specific band at M(r) 36 000 for the three anti-sera. Western blotting showed that the three anti-sera all specifically recognized rGiardin.</p><p><strong>Conclusion: </strong>Immunization with the KLH-G1, KLH-G2, and KLH-G3 conjugates induced production of specific IgG antibody in rabbits, which can recognize rGiardin.</p>\",\"PeriodicalId\":23981,\"journal\":{\"name\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"volume\":\"34 5\",\"pages\":\"389-93\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:鉴定蓝氏贾第鞭毛虫α-8贾第丁的显性表位,并分析其免疫反应性。方法:采用DNAstar、Biosun和CLUSTAL W软件进行生物信息学分析,预测α-8贾丁苷的优势表位G1(7-17 aa)、G2(30-40 aa)和G3(296-306 aa)。每个表位与keyhole limpethemocyanin (KLH)偶联,通过背部多点(8-10点)皮下注射(偶联物0.5 mg /只,每个点100 μl)免疫雌性鼠兔。在第一次免疫后的第14、21、28天,以0.2 mg偶联物/只的剂量注射。每次免疫前采血,末次免疫后第7天采血颈动脉50 ml。采用间接ELISA法测定抗klh - g1、抗klh - g2和抗klh - g3血清的抗体滴度。采用免疫印迹法(Western blotting)分析3种抗血清对推荐的紫荆苷(rGiardin)的反应性。结果:纯化的偶联物KLH-G1、KLH-G2、KLH-G3的浓度分别为0.66、0.95、0.25 mg/ml。ELISA结果显示,抗klh - g1、抗klh - g2、抗klh - g3血清的抗体效价分别为1∶12800、1∶51200、1∶51200。SDS-PAGE显示这三种抗血清在M(r) 36000处有特异条带。Western blotting结果显示,3种抗血清均特异性识别rGiardin。结论:用KLH-G1、KLH-G2和KLH-G3偶联物免疫家兔可产生特异性IgG抗体,该抗体可识别栀子苷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Antigenic Characterization of Immunodominant Epitopes of Alpha-8 giardin in Giardia lamblia].

Objective: To identify the dominant epitopes of α-8 giardin in Giardia lamblia, and analyze their immunoreactivity.

Methods: Three dominant epitopes G1(7-17 aa), G2(30-40 aa) and G3(296-306 aa) were predicted for α-8 giardin by bioinformatic analysis using DNAstar, Biosun and CLUSTAL W softwares. Each epitope was conjugated to keyhole limpethemocyanin (KLH) and then used to immunize female Chinchilla rabbits via multi-point(8-10 points) subcutaneous injections on the back(0.5 mg conjugate/rabbit, 100 μl at each point). Then the rabbits were boosted(0.2 mg conjugate/rabbit) on days 14, 21 and 28 after the first immunization. Blood was collected prior to each immunization, and carotid artery blood(50 ml) was collected on day 7 after the last immunization. The antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was determined with indirect ELISA. The reactivity of the three anti-sera with recominant giardin (rGiardin) was analyzed with Western blotting.

Results: The concentration of the purified conjugates KLH-G1, KLH-G2, and KLH-G3 was 0.66, 0.95 and 0.25 mg/ml, respectively. ELISA showed that the antibody titer for anti-KLH-G1, anti-KLH-G2 and anti-KLH-G3 sera was 1∶12800, 1∶51200, 1∶51200, respectively. SDS-PAGE revealed a specific band at M(r) 36 000 for the three anti-sera. Western blotting showed that the three anti-sera all specifically recognized rGiardin.

Conclusion: Immunization with the KLH-G1, KLH-G2, and KLH-G3 conjugates induced production of specific IgG antibody in rabbits, which can recognize rGiardin.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信