Rabbit antipeptide antibodies against restricted domains of the histocompatibility complex.

A Chersi, R A Houghten
{"title":"Rabbit antipeptide antibodies against restricted domains of the histocompatibility complex.","authors":"A Chersi,&nbsp;R A Houghten","doi":"10.1515/znc-1984-0621","DOIUrl":null,"url":null,"abstract":"<p><p>The work reported here concerns the specificity of four antibodies elicited by synthetic peptides corresponding to three domains of the HLA-B7 glycoprotein, and one of the beta 2 microglobulin. One of the four peptides had been previously investigated, but the data obtained by its elicited antibodies were uncomplete. Of the three HLA-B7 peptides assayed, one was unable to raise an immune response. The other two produced antibodies in good titer that reacted with the antigen peptide, but were unable to recognize antigenic determinants when tested on membrane glycoproteins solubilized from human lymphoblastoid cells. In contract, the antibody elicited by the only fragment from the beta 2microglobulin recognized the native beta 2microglobulin molecule as well as HLA/beta 2m complexes, and reacted with intact human cells, as determined by ELISA and by FACS analysis. This peptide, which contains one of the most hydrophylic fragment of the whole molecule, is likely an important antigenic site, since it is also recognized by traditional antisera raised against native beta 2microglobulin.</p>","PeriodicalId":23914,"journal":{"name":"Zeitschrift fur Naturforschung. Section C, Biosciences","volume":"39 6","pages":"646-51"},"PeriodicalIF":0.0000,"publicationDate":"1984-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1515/znc-1984-0621","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift fur Naturforschung. Section C, Biosciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/znc-1984-0621","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

The work reported here concerns the specificity of four antibodies elicited by synthetic peptides corresponding to three domains of the HLA-B7 glycoprotein, and one of the beta 2 microglobulin. One of the four peptides had been previously investigated, but the data obtained by its elicited antibodies were uncomplete. Of the three HLA-B7 peptides assayed, one was unable to raise an immune response. The other two produced antibodies in good titer that reacted with the antigen peptide, but were unable to recognize antigenic determinants when tested on membrane glycoproteins solubilized from human lymphoblastoid cells. In contract, the antibody elicited by the only fragment from the beta 2microglobulin recognized the native beta 2microglobulin molecule as well as HLA/beta 2m complexes, and reacted with intact human cells, as determined by ELISA and by FACS analysis. This peptide, which contains one of the most hydrophylic fragment of the whole molecule, is likely an important antigenic site, since it is also recognized by traditional antisera raised against native beta 2microglobulin.

兔抗组织相容性复合体限制结构域的抗肽抗体。
本文报道的工作涉及由与HLA-B7糖蛋白的三个结构域和β 2微球蛋白的一个结构域相对应的合成肽引发的四种抗体的特异性。四种肽中的一种先前已被研究过,但其诱导的抗体获得的数据是不完整的。在检测的三种HLA-B7肽中,有一种无法引起免疫反应。另外两种产生的抗体滴度高,能与抗原肽反应,但在人淋巴母细胞溶解的膜糖蛋白上检测时,不能识别抗原决定因素。相反,通过ELISA和FACS分析,β 2微球蛋白唯一片段引发的抗体识别天然β 2微球蛋白分子和HLA/ β 2复合物,并与完整的人细胞发生反应。该肽含有整个分子中最亲水的片段之一,可能是一个重要的抗原位点,因为它也被传统的抗血清所识别,以对抗天然β 2微球蛋白。
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
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