Suppr超能文献

插入到麦芽糖结合蛋白(MalE蛋白)允许位点的HIV-1 gp41表位ELDKWA的抗原性和免疫原性

Antigenicity and immunogenicity of the HIV-1 gp41 epitope ELDKWA inserted into permissive sites of the MalE protein.

作者信息

Coëffier E, Clément J M, Cussac V, Khodaei-Boorane N, Jehanno M, Rojas M, Dridi A, Latour M, El Habib R, Barré-Sinoussi F, Hofnung M, Leclerc C

机构信息

Unité de Biologie des Régulations Immunitaires, Institut Pasteur 25, rue du Docteur Roux, 75724, Cedex 15, Paris, France.

出版信息

Vaccine. 2000 Nov 22;19(7-8):684-93. doi: 10.1016/s0264-410x(00)00267-x.

Abstract

The highly conserved amino acid sequence ELDKWA of HIV-1 gp41 has been inserted into Escherichia coli MalE protein which had been shown to be an adequate carrier to present foreign epitopes to the immune system. We first investigated whether eight different permissive sites of MalE are able to tolerate an insertion of 7-50 residues encoding this epitope. Secondly, antigenicity of the epitope inserted in MalE protein was estimated from monoclonal antibody 2F5 binding analysis using the BIAcore(R) technology and its immunogenicity in mice was measured as the ability of hybrid proteins to elicit antibodies against a synthetic peptide containing this epitope. This study revealed a good correlation between the antigenicity of the inserted epitope and its immunogenicity. Increasing the length of the inserted epitope, as well as inserting multicopies of this epitope increased both its antigenicity and immunogenicity. However, none of the MalE hybrid proteins tested induced anti-HIV-1 neutralizing antibodies. This study strongly suggests that the capacity of the 2F5 epitope to induce neutralizing antibodies depends on the molecular context in which it is presented.

摘要

已将HIV-1 gp41高度保守的氨基酸序列ELDKWA插入大肠杆菌MalE蛋白中,该蛋白已被证明是向免疫系统呈递外源表位的合适载体。我们首先研究了MalE的八个不同允许位点是否能够耐受编码该表位的7至50个残基的插入。其次,使用BIAcore®技术通过单克隆抗体2F5结合分析评估插入MalE蛋白中的表位的抗原性,并测定其在小鼠中的免疫原性,以此衡量杂合蛋白引发针对含有该表位的合成肽的抗体的能力。本研究揭示了插入表位的抗原性与其免疫原性之间具有良好的相关性。增加插入表位的长度以及插入该表位的多个拷贝均会增加其抗原性和免疫原性。然而,所测试的MalE杂合蛋白均未诱导出抗HIV-1中和抗体。本研究有力地表明,2F5表位诱导中和抗体的能力取决于其呈现的分子环境。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验