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促红细胞生成素特异性多克隆抗体的制备。

Production of Erythropoietin-Specific Polyclonal Antibodies.

作者信息

Maboudi Kourosh, Hosseini Seyedeh Marzieh, Sepahi Mina, Yaghoubi Hashem, Hadadian Shahin

机构信息

Department of Biochemistry, Ardabil Branch, Islamic Azad University, Ardabil, 3159915111, Iran.

Quality Control Department, Pasteur Institute of Iran, Karaj, 31635/157, Iran.

出版信息

Iran J Biotechnol. 2017 Mar;15(1):50-57. doi: 10.15171/ijb.1413.

Abstract

BACKGROUND

Erythropoietin, as a principal hormone promotes red blood cell production in bone marrow. Varieties of erythropoietin biosimilar are being produced by recombinant DNA technology in cell cultures. The detection or quantifi cation of these molecules are being performed by diff erent methods which some of theme such as Western blot and enzymelinked immunosorbent assay (ELISA) require specifi c antibodies. High cost, inappropriate shipping (cold chain failures), reduced sensitivity and thus poor detection performance are common pitfalls of using commercial kits for performing immunological tests.

OBJECTIVES

To produce in-house polyclonal antibody against active pharmaceutical ingredient (API) of recombinant human erythropoietin (rh-EPO) was the aim of this study.

MATERIALS AND METHODS

Two healthy female albino rabbits were injected four times in 14 days interval using rh-EPO API as antigen. The produced antibody was separated from plasma via either caprylic acid or saturated ammonium sulfate precipitation and the results were compared from each purification methodologies. The antibody was further purified by ion exchange chromatography. Acceptable purity and good immunogenicity were detected respectively by SDS-PAGE and western blot analysis. The purified antibody was compared with a commercial kit to determine rh-EPO concentration in diff erent steps of production batches via ELISA.

RESULTS

The purity of antibodies after ion exchange chromatography, obtained from caprylic acid and ammonium sulfate precipitation were 97 and 80%, respectively.

CONCLUSIONS

As producing in house kits is one of the important challenges of bio- pharmaceutical manufacturers, a simple, cost- and time-effective, and easy to scale up strategy for making in-house polyclonal antibody was set up. Caprylic acid precipitation resulted higher purity than ammonium sulfate and fi nally purified antibody (97% purity) used as a capture antibody in sandwich ELISA test was able to detect erythropoietin antigen as sensitive (100%) and specifi c (100%) as commercial kits.

摘要

背景

促红细胞生成素是促进骨髓中红细胞生成的主要激素。多种促红细胞生成素生物类似物通过重组DNA技术在细胞培养物中生产。这些分子的检测或定量通过不同方法进行,其中一些方法如蛋白质印迹法和酶联免疫吸附测定(ELISA)需要特异性抗体。使用商业试剂盒进行免疫检测常见的问题包括成本高、运输不当(冷链故障)、灵敏度降低以及检测性能差。

目的

本研究的目的是制备针对重组人促红细胞生成素(rh-EPO)活性药物成分(API)的自制多克隆抗体。

材料和方法

以rh-EPO API为抗原,对两只健康雌性白化兔每隔14天注射一次,共注射四次。通过辛酸或饱和硫酸铵沉淀从血浆中分离产生的抗体,并比较每种纯化方法的结果。通过离子交换色谱进一步纯化抗体。分别通过SDS-PAGE和蛋白质印迹分析检测抗体的纯度和免疫原性。将纯化的抗体与商业试剂盒进行比较,通过ELISA测定生产批次不同步骤中的rh-EPO浓度。

结果

通过辛酸沉淀和硫酸铵沉淀获得的离子交换色谱后抗体纯度分别为97%和80%。

结论

由于自制试剂盒是生物制药制造商面临的重要挑战之一,因此建立了一种简单、经济高效且易于扩大规模的自制多克隆抗体制备策略。辛酸沉淀比硫酸铵沉淀得到的纯度更高,最终纯化的抗体(纯度97%)用作夹心ELISA试验中的捕获抗体,能够像商业试剂盒一样灵敏(100%)且特异(100%)地检测促红细胞生成素抗原。

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