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Isolation of sequences from a random-sequence expression library that mimic viral epitopes.从模拟病毒表位的随机序列表达文库中分离序列。
J Immunol Methods. 1992 Aug 10;152(2):149-57. doi: 10.1016/0022-1759(92)90136-h.
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本文引用的文献

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Solubilization and immune-detection of beta-galactosidase hybrid proteins carrying foreign antigenic determinants.携带外源抗原决定簇的β-半乳糖苷酶杂合蛋白的溶解及免疫检测。
Nucleic Acids Res. 1983 Jun 25;11(12):4077-92. doi: 10.1093/nar/11.12.4077.
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Construction of a new family of high efficiency bacterial expression vectors: identification of cDNA clones coding for human liver proteins.新型高效细菌表达载体家族的构建:编码人肝蛋白的cDNA克隆的鉴定
EMBO J. 1984 Jun;3(6):1429-34. doi: 10.1002/j.1460-2075.1984.tb01988.x.
3
The nucleotide sequence of the peplomer gene of porcine transmissible gastroenteritis virus (TGEV): comparison with the sequence of the peplomer protein of feline infectious peritonitis virus (FIPV).猪传染性胃肠炎病毒(TGEV)纤突蛋白基因的核苷酸序列:与猫传染性腹膜炎病毒(FIPV)纤突蛋白序列的比较。
Virus Res. 1987 Nov;8(4):363-71. doi: 10.1016/0168-1702(87)90008-6.
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Structural and functional approaches to the study of protein antigenicity.
Immunol Today. 1989 Aug;10(8):266-72. doi: 10.1016/0167-5699(89)90140-0.
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Antigenicity of the peplomer protein of infectious bronchitis virus.传染性支气管炎病毒纤突蛋白的抗原性
Mol Immunol. 1989 Jan;26(1):7-15. doi: 10.1016/0161-5890(89)90014-x.
6
Antigenic structure of the E2 glycoprotein from transmissible gastroenteritis coronavirus.传染性胃肠炎冠状病毒E2糖蛋白的抗原结构
Virus Res. 1988 Apr;10(1):77-93. doi: 10.1016/0168-1702(88)90059-7.
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Three-dimensional structure of poliovirus serotype 1 neutralizing determinants.脊髓灰质炎病毒1型中和决定簇的三维结构
J Virol. 1988 May;62(5):1781-94. doi: 10.1128/JVI.62.5.1781-1794.1988.
8
Topological mapping of complement component C9 by recombinant DNA techniques suggests a novel mechanism for its insertion into target membranes.通过重组DNA技术对补体成分C9进行拓扑图谱分析,提示了其插入靶膜的一种新机制。
EMBO J. 1987 Jul;6(7):1951-7. doi: 10.1002/j.1460-2075.1987.tb02457.x.
9
A priori delineation of a peptide which mimics a discontinuous antigenic determinant.模拟不连续抗原决定簇的肽的先验描绘。
Mol Immunol. 1986 Jul;23(7):709-15. doi: 10.1016/0161-5890(86)90081-7.
10
Antigenic structure of transmissible gastroenteritis virus. II. Domains in the peplomer glycoprotein.传染性胃肠炎病毒的抗原结构。II. 纤突糖蛋白中的结构域。
J Gen Virol. 1986 Jul;67 ( Pt 7):1405-18. doi: 10.1099/0022-1317-67-7-1405.

从模拟病毒表位的随机序列表达文库中分离序列。

Isolation of sequences from a random-sequence expression library that mimic viral epitopes.

作者信息

Lenstra J A, Erkens J H, Langeveld J G, Posthumus W P, Meloen R H, Gebauer F, Correa I, Enjuanes L, Stanley K K

机构信息

Institute of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht, Netherlands.

出版信息

J Immunol Methods. 1992 Aug 10;152(2):149-57. doi: 10.1016/0022-1759(92)90136-h.

DOI:10.1016/0022-1759(92)90136-h
PMID:1380046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7131437/
Abstract

We describe the use of random peptide sequences for the mapping of antigenic determinants. An oligonucleotide with a completely degenerate sequence of 17 or 23 nucleotides was inserted into a bacterial expression vector. This resulted in an expression library producing random hexa- or octapeptides attached to a beta-galactosidase hybrid protein. Mimotopes, or antigenic sequences that mimic an epitope, were selected by immunoscreening of colonies with monoclonal antibodies, which were specific for antigenic sites on the spike protein of the coronavirus transmissible gastroenteritis virus. We report one mimotope for antigenic site II, eight for site III and one for site IV. The site III and site IV mimotopes were closely similar to the corresponding linear epitopes, localized previously in the amino acid sequence of the S protein. An alignment of the site II mimotope and the sequence of the S protein around Trp97, which is substituted in escape mutants, suggests that this mimotope mimics a conformational epitope located around residues 97-103. Applications of mimotopes to epitope mapping, serodiagnosis and vaccine development are discussed.

摘要

我们描述了使用随机肽序列绘制抗原决定簇的方法。将一个具有17或23个核苷酸完全简并序列的寡核苷酸插入细菌表达载体中。这产生了一个表达文库,该文库产生与β-半乳糖苷酶杂合蛋白相连的随机六肽或八肽。通过用针对传染性胃肠炎冠状病毒刺突蛋白抗原位点的单克隆抗体对菌落进行免疫筛选,选择模拟表位或模拟抗原表位的抗原序列。我们报告了一个针对抗原位点II的模拟表位、八个针对位点III的模拟表位和一个针对位点IV的模拟表位。位点III和位点IV的模拟表位与先前定位在S蛋白氨基酸序列中的相应线性表位非常相似。位点II模拟表位与S蛋白在Trp97周围的序列比对(Trp97在逃逸突变体中被取代)表明,该模拟表位模拟了位于97-103位残基周围的构象表位。文中讨论了模拟表位在表位定位、血清学诊断和疫苗开发中的应用。