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针对排泄分泌重组抗原的人单克隆抗体蛋白的分离与制备

Isolation and Production of Human Monoclonal Antibody Proteins against a Excretory-Secretory Recombinant Antigen.

作者信息

Baharudeen Zamrina, Noordin Rahmah, Soon Lim Theam, Balachandra Dinesh, Anuar Nor Suhada, Mustafa Fatin Hamimi, Rahumatullah Anizah

机构信息

Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, Penang 11800, Malaysia.

出版信息

Pathogens. 2022 Oct 25;11(11):1232. doi: 10.3390/pathogens11111232.

Abstract

Toxocariasis is a widespread zoonotic parasitic disease with a significant socioeconomic impact, particularly on underprivileged communities. Limitations of existing diagnostic tools and vague presenting symptoms may lead to misdiagnosis, thus underestimating the actual global impact of the disease. The present study describes the isolation and production of novel recombinant monoclonal antibodies against Toxocara canis recombinant TES-26 antigen (rTES-26) utilizing a human helminth scFv phage display library. The isolated antibody clones were characterized based on their gene sequences and binding characteristics. Three clones representing unique gene families (clone 48: IgHV3-LV1; clone 49: IgHV3-LV3; clone 50: IgHV6-LV3) were isolated, but only clones 48 and 49 showed successful insertion of the full-length scFv antibody sequence after sub-cloning. Both clones produced antibody proteins of good solubility and satisfactory yield and purity. Binding assays via Western blot and ELISA using rTES-26 and Toxocara canis native protein showed that both monoclonal antibodies were highly specific and sensitive to the target antigen. A preliminary antigen detection ELISA showed the diagnostic potential of the monoclonal antibody proteins. The proteins can also be useful in studying host−parasite interactions and therapeutic applications.

摘要

弓首蛔虫病是一种广泛传播的人畜共患寄生虫病,具有重大的社会经济影响,对贫困社区的影响尤为显著。现有诊断工具的局限性和模糊的症状表现可能导致误诊,从而低估了该疾病在全球的实际影响。本研究描述了利用人源蠕虫单链抗体可变区(scFv)噬菌体展示文库,分离并制备针对犬弓首蛔虫重组TES-26抗原(rTES-26)的新型重组单克隆抗体。根据分离出的抗体克隆的基因序列和结合特性对其进行表征。分离出了代表独特基因家族的三个克隆(克隆48:IgHV3-LV1;克隆49:IgHV3-LV3;克隆50:IgHV6-LV3),但亚克隆后只有克隆48和49成功插入了全长scFv抗体序列。这两个克隆均产生了溶解性良好、产量和纯度令人满意的抗体蛋白。使用rTES-26和犬弓首蛔虫天然蛋白通过蛋白质印迹法和酶联免疫吸附测定法进行的结合试验表明,这两种单克隆抗体对靶抗原具有高度特异性和敏感性。初步的抗原检测酶联免疫吸附测定显示了单克隆抗体蛋白的诊断潜力。这些蛋白在研究宿主-寄生虫相互作用及治疗应用方面也可能有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc04/9698333/b94a9a876dbe/pathogens-11-01232-g001.jpg

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