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[抗李斯特菌溶血素O单克隆抗体的制备与鉴定]

[Perparation and characterization of the monoclonal antibodies against listeriolysin O].

作者信息

Dong Hui, Jiao Xin-an, Yin Yue-lan, Pan Zhi-ming, Huang Jin-lin

机构信息

Renal Department of Daping Hospital Chongqing 400042, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2008 Mar;24(3):240-2.

Abstract

AIM

To prepare the monoclonal antibodies (mAbs) against listeriolysin O (LLO), which is the major virulence factor of Listeria monocytogenes.

METHODS

The BALB/c mice were immunized with the SDS-PAGE product of BL21(pGEX-6p-1-hly). The purified LLO-GST protein was used as antigen for detection. mAbs against LLO were prepared by using the lymphocyte hybridoma technique. The specificity of mAbs was characterized by Dot-ELISA and Western blot.

RESULTS

Three hybridoma cell lines named 3B6, 4D1 and 5D10 secreting mAbs against LLO were obtained. The immunoglobulin subclasses of the mAbs were IgG1. The ELISA titer of the ascitic fluids of 3B6, 4D1 and 5D10 was 1:200,000, 1:200,000 and 1:100,000, respectively. Western blot analysis confirmed the three mAbs reacted on fusion protein LLO-GST but didn't react on protein GST. Dot-ELISA proved the three mAbs only react on the bacteria expressing LLO.

CONCLUSION

The successful preparation of three mAbs specific to protein LLO lays a foundation for further study of the biological characteristics of LLO and the pathogenesis of Listeria monocytogenes.

摘要

目的

制备抗李斯特菌溶血素O(LLO)的单克隆抗体,LLO是单核细胞增生李斯特菌的主要毒力因子。

方法

用BL21(pGEX-6p-1-hly)的SDS-PAGE产物免疫BALB/c小鼠。纯化的LLO-GST蛋白用作检测抗原。采用淋巴细胞杂交瘤技术制备抗LLO的单克隆抗体。通过斑点酶联免疫吸附测定(Dot-ELISA)和蛋白质免疫印迹法鉴定单克隆抗体的特异性。

结果

获得了3株分泌抗LLO单克隆抗体的杂交瘤细胞系,分别命名为3B6、4D1和5D10。这些单克隆抗体的免疫球蛋白亚类为IgG1。3B6、4D1和5D10腹水的酶联免疫吸附测定(ELISA)效价分别为1:200,000、1:200,000和1:100,000。蛋白质免疫印迹分析证实这3种单克隆抗体与融合蛋白LLO-GST反应,但不与GST蛋白反应。斑点酶联免疫吸附测定证明这3种单克隆抗体仅与表达LLO的细菌反应。

结论

成功制备了3种针对LLO蛋白的单克隆抗体,为进一步研究LLO的生物学特性和单核细胞增生李斯特菌的致病机制奠定了基础。

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