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烟草植株中抗MUC1粘蛋白重组单域单克隆抗体的表达与特性分析

Expression and characterization of a recombinant single-domain monoclonal antibody against MUC1 mucin in tobacco plants.

作者信息

Rajabi-Memari H, Jalali-Javaran M, Rasaee M J, Rahbarizadeh F, Forouzandeh-Moghadam M, Esmaili A

机构信息

Department of Plant Breeding, School of Agriculture, Tarbiat Modares University, Tehran, Iran.

出版信息

Hybridoma (Larchmt). 2006 Aug;25(4):209-15. doi: 10.1089/hyb.2006.25.209.

Abstract

A promising alternative to conventional antibodies is the single-domain antibody fragment of the Camelidae (V(HH)), which (because of features such as small length, high expression, solubility, and stability) is preferred to other antibody derivatives. In this report, a recombinant single-domain antibody (V(HH)) against MUC1 mucin in the tobacco plant, which may be considered as a suitable and economical alternative expression system, was produced. This antibody was expressed under the control of a strong constitutive promoter, CaMV35S, and NOS terminator. A plant high-expression sequence (Kozak sequence) was linked at the 5' end for overexpression of the V(HH) gene. The constructed cassette (pBIV(HH)) was transferred to agrobacterium, and the VHH gene was inserted into the plant genome by agrobacterium-mediated transformation. Transgenic lines were selected on kanamycin (100 mg/L) and maintained in soil, and subsequent generations were obtained. The presence and expression of the transgene was confirmed in the transformants by polymerase chain reaction (PCR), enzyme-linked immunosorbent assay (ELISA), and Western blot. Tobacco transgenic lines leave expressed V(HH) at levels varying from 1.12% to 1.63% of the total soluble protein. This report examines the transformation and expression of recombinant single-domain antibody (V(HH)) against antigen-associated tumor in tobacco plants.

摘要

骆驼科动物的单域抗体片段(V(HH))是传统抗体的一种有前景的替代物,因其长度小、高表达、溶解性和稳定性等特点,比其他抗体衍生物更受青睐。在本报告中,在烟草植物中产生了一种针对MUC1粘蛋白的重组单域抗体(V(HH)),烟草植物可被视为一种合适且经济的替代表达系统。该抗体在强组成型启动子CaMV35S和NOS终止子的控制下表达。在5'端连接了一个植物高表达序列(科扎克序列)以实现V(HH)基因的过表达。构建的盒式载体(pBIV(HH))被转移到农杆菌中,VHH基因通过农杆菌介导的转化插入植物基因组。在卡那霉素(100 mg/L)上筛选转基因株系并在土壤中培养,获得了后续世代。通过聚合酶链反应(PCR)、酶联免疫吸附测定(ELISA)和蛋白质印迹法在转化体中确认了转基因的存在和表达。烟草转基因株系叶片中V(HH)的表达水平占总可溶性蛋白的1.12%至1.63%。本报告研究了针对抗原相关肿瘤的重组单域抗体(V(HH))在烟草植物中的转化和表达。

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