免疫球蛋白cDNA重链可变区扩增的退化引物设计

Wang Ying, Chen Wei, Li Xu, Cheng Bing
{"title":"免疫球蛋白cDNA重链可变区扩增的退化引物设计","authors":"Wang Ying, Chen Wei, Li Xu, Cheng Bing","doi":"10.1109/IMSCCS.2006.53","DOIUrl":null,"url":null,"abstract":"The amplification of variable regions (Fv) of immunoglobulins (Ig) becomes a major challenge in cloning antibody genes either from hybridoma cell lines or splenic B cells. When we amplified the heavy-chain variable regions (VH) gene from one hybridoma cell line which were not amplified successfully under conventional protocols, a novel method was developed to design the degenerated primer of immunoglobulin cDNA and rapid amplification of cDNA ends polymerase chain reaction (RACE PCR) protocols were performed to recognize the VH gene from the hybridoma cell line. The most highly conserved region in the middle of the VH regions of the Ig cDNA was identified and a degenerated 5'primer was designed using our algorithms. The VH gene was amplified by the 3'RACE and 5'RACE. The VH sequence of CSA cells was 399 bp. The new protocol rescued the amplifications of the VH gene that had failed under conventional protocols and notably increased amplification specificity. The algorithm improved the primer design efficiency and is useful in building VH and VL gene libraries or cloning of unknown genes in gene families","PeriodicalId":202629,"journal":{"name":"First International Multi-Symposiums on Computer and Computational Sciences (IMSCCS'06)","volume":"6 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2006-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Degenerated Primer Design to Amplify the Heavy Chain Variable Region from Immunoglobulin cDNA\",\"authors\":\"Wang Ying, Chen Wei, Li Xu, Cheng Bing\",\"doi\":\"10.1109/IMSCCS.2006.53\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The amplification of variable regions (Fv) of immunoglobulins (Ig) becomes a major challenge in cloning antibody genes either from hybridoma cell lines or splenic B cells. When we amplified the heavy-chain variable regions (VH) gene from one hybridoma cell line which were not amplified successfully under conventional protocols, a novel method was developed to design the degenerated primer of immunoglobulin cDNA and rapid amplification of cDNA ends polymerase chain reaction (RACE PCR) protocols were performed to recognize the VH gene from the hybridoma cell line. The most highly conserved region in the middle of the VH regions of the Ig cDNA was identified and a degenerated 5'primer was designed using our algorithms. The VH gene was amplified by the 3'RACE and 5'RACE. The VH sequence of CSA cells was 399 bp. The new protocol rescued the amplifications of the VH gene that had failed under conventional protocols and notably increased amplification specificity. The algorithm improved the primer design efficiency and is useful in building VH and VL gene libraries or cloning of unknown genes in gene families\",\"PeriodicalId\":202629,\"journal\":{\"name\":\"First International Multi-Symposiums on Computer and Computational Sciences (IMSCCS'06)\",\"volume\":\"6 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"First International Multi-Symposiums on Computer and Computational Sciences (IMSCCS'06)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/IMSCCS.2006.53\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"First International Multi-Symposiums on Computer and Computational Sciences (IMSCCS'06)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/IMSCCS.2006.53","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

免疫球蛋白(Ig)可变区(Fv)的扩增是从杂交瘤细胞系或脾B细胞中克隆抗体基因的主要挑战。短句来源本文从一株传统方法无法扩增的杂交瘤细胞株中扩增出重链可变区(VH)基因,提出了一种设计免疫球蛋白cDNA退化引物的新方法,并采用cDNA末端快速扩增聚合酶链反应(RACE PCR)技术对该杂交瘤细胞株中的VH基因进行了识别。在Ig cDNA的VH区中间找到了高度保守的区域,并利用我们的算法设计了一个退化的5'引物。通过3'RACE和5'RACE扩增VH基因。CSA细胞的VH序列为399 bp。新方案挽救了在传统方案下失败的VH基因扩增,并显着提高了扩增特异性。该算法提高了引物设计效率,可用于构建VH和VL基因文库或克隆基因家族中未知基因
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Degenerated Primer Design to Amplify the Heavy Chain Variable Region from Immunoglobulin cDNA
The amplification of variable regions (Fv) of immunoglobulins (Ig) becomes a major challenge in cloning antibody genes either from hybridoma cell lines or splenic B cells. When we amplified the heavy-chain variable regions (VH) gene from one hybridoma cell line which were not amplified successfully under conventional protocols, a novel method was developed to design the degenerated primer of immunoglobulin cDNA and rapid amplification of cDNA ends polymerase chain reaction (RACE PCR) protocols were performed to recognize the VH gene from the hybridoma cell line. The most highly conserved region in the middle of the VH regions of the Ig cDNA was identified and a degenerated 5'primer was designed using our algorithms. The VH gene was amplified by the 3'RACE and 5'RACE. The VH sequence of CSA cells was 399 bp. The new protocol rescued the amplifications of the VH gene that had failed under conventional protocols and notably increased amplification specificity. The algorithm improved the primer design efficiency and is useful in building VH and VL gene libraries or cloning of unknown genes in gene families
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:481959085
Book学术官方微信