异源表达、纯化和生成 Annexin A8 的特异性抗体。

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Zexin Lin , Wei Sun , Xuemei Zhao , Yang Chen , Kerry M. Loomes , Hongbo Li , Hannah Xiaoyan Hui , Donghai Wu
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引用次数: 0

摘要

膜联蛋白A8(ANXA8)是膜联蛋白基因家族的一员,在多种肿瘤组织中均有高水平的mRNA和蛋白表达,是潜在的肿瘤生物标志物。在本研究中,我们建立了一种酶联免疫吸附试验(ELISA)来特异性检测ANXA8的存在并准确测定其浓度。为此,我们使用毕赤酵母和大肠杆菌表达系统表达了一系列蛋白质。其中,以毕赤酵母中表达的人源ANXA8作为抗原和抗体筛选,以毕赤酵母中表达的人源ANXA2和ANXA5以及大肠杆菌BL21(DE3)中表达的鼠源ANXA8作为反筛,消除交叉反应抗体,筛选人源和鼠源对ANXA8具有特异性的抗体。通过重组蛋白的制备纯化、免疫、特异性筛选和表位配对选择等研究,获得了两种特异性单克隆抗体E9和B7,它们明显针对ANXA8的不同表位。以ANXA8为阳性对照,对重组人ANXA2和ANXA5进行特异性检测。Western Blot和Sandwich ELISA均具有较高的灵敏度和特异性,后者的检出限约为0.065 ng/mL。综上所述,本研究为定量测定ANXA8的浓度和监测疾病进展的潜在肿瘤生物标志物提供了实验工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Heterologous expression, purification and generation of specific antibodies for Annexin A8

Heterologous expression, purification and generation of specific antibodies for Annexin A8
Annexin A8 (ANXA8) is a member of the Annexin gene family, with high levels of its mRNA and protein observed in various tumor tissues, making it a potential tumor biomarker. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) to specifically detect the presence and accurately determine the concentration of ANXA8. To this end, we expressed a series of proteins using both Pichia pastoris and Escherichia coli expression systems. Particularly, human ANXA8 expressed in Pichia pastoris was used as the antigen and for antibody screening, while human ANXA2 and ANXA5 expressed in Pichia pastoris and murine ANXA8 expressed in E. coli BL21 (DE3) were used as counter screens to eliminate cross-reactive antibodies and to select antibodies that show specificity to ANXA8 from both human and mouse. Through research efforts with production and purification of recombinant proteins, immunization, specificity screening and selection of epitope pairing, two specific monoclonal antibodies, E9 and B7, apparently targeting different epitopes of ANXA8, were obtained. The specificity of the antibody pair was checked against recombinant human ANXA2 and ANXA5 with ANXA8 as the positive control. Western Blot and Sandwich ELISA demonstrate superb sensitivity and specificity with a detection limit of about 0.065 ng/mL for the latter. In summary, this study provides an experimental tool for the quantitative determination of ANXA8 concentration and a potential tumor biomarker to monitor disease progression.
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来源期刊
Protein expression and purification
Protein expression and purification 生物-生化研究方法
CiteScore
3.70
自引率
6.20%
发文量
120
审稿时长
32 days
期刊介绍: Protein Expression and Purification is an international journal providing a forum for the dissemination of new information on protein expression, extraction, purification, characterization, and/or applications using conventional biochemical and/or modern molecular biological approaches and methods, which are of broad interest to the field. The journal does not typically publish repetitive examples of protein expression and purification involving standard, well-established, methods. However, exceptions might include studies on important and/or difficult to express and/or purify proteins and/or studies that include extensive protein characterization, which provide new, previously unpublished information.
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