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Production of a human single-chain variable fragment antibody against esophageal carcinoma

机译:抗食管癌的人单链可变片段抗体的生产

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摘要

AIM: To construct a phage display library of human single-chain variable fragment (scFv) antibodies associated with esophageal cancer and to preliminarily screen a scFv antibody against esophageal cancer.METHODS: Total RNA extracted from metastatic lymph nodes of esophageal cancer patients was used to construct a scFv gene library. Rescued by M13K07 helper phage, the scFv phage display library was constructed. esophageal cancer cell line Eca109 and normal human esophageal epithelial cell line (NHEEC) were used for panning and subtractive panning of the scFv phage display library to obtain positive phage clones. Soluble scFv was expressed in E. coli HB2151 which was transfected with the positive phage clone, then purified by affinity chromatography. Relative molecular mass of soluble scFv was estimated by Western blotting, its bioactivity was detected by cell ELISA assay. Sequence of scFv was determined using the method of dideoxynucleotide sequencing.RESULTS: The size of scFv gene library was approximately 9 × 106 clones. After four rounds of panning with Eca109 and three rounds of subtractive panning with NHEEC cells, 25 positive phage clones were obtained. Soluble scFv was found to have a molecular mass of 31 ku and was able to bind to Eca109 cells, but not to HeLa and NHEEC cells. Variable heavy (VH) gene from one of the positive clones was shown to be derived from the γ chain subgroup IV of immunoglobulin, and variable light (VL) gene from the κ chain subgroup I of immunoglobulin.CONCLUSION: A human scFv phage display library can be constructed from the metastatic lymph nodes of esophageal cancer patients. A whole human scFv against esophageal cancer shows some bioactivity.
机译:目的:构建与食管癌相关的人单链可变片段(scFv)抗体的噬菌体展示文库,并初步筛选抗食管癌的scFv抗体。方法:采用食管癌患者转移淋巴结中提取的总RNA进行检测。构建scFv基因文库。在M13K07辅助噬菌体的帮助下,构建了scFv噬菌体展示文库。食管癌细胞系Eca109和正常人食道上皮细胞系(NHEEC)用于scFv噬菌体展示文库的淘选和减价淘选以获得阳性噬菌体克隆。可溶性scFv在大肠杆菌HB2151中表达,用阳性噬菌体克隆转染,然后通过亲和层析纯化。通过蛋白质印迹法测定可溶性scFv的相对分子量,并通过细胞ELISA测定法检测其生物活性。结果:scFv基因文库的大小约为9×10 6 克隆。用Eca109进行四轮淘选和使用NHEEC细胞进行三轮减性淘选后,获得了25个阳性噬菌体克隆。发现可溶性scFv的分子量为31 ku,能够与Eca109细胞结合,但不能与HeLa和NHEEC细胞结合。结论:一个人scFv噬菌体展示文库显示出来自一个阳性克隆的可变重(VH)基因来自免疫球蛋白的γ链IV亚组,可变轻(VL)基因来自免疫球蛋白的κ链亚组。可以从食道癌患者的转移性淋巴结中构建。整个人类针对食道癌的scFv表现出一定的生物活性。

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