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抗恶性黑素瘤单链抗体-鱼精蛋白融合蛋白表达载体的构建及评价

王昊 杨一飞 王炜 管冰 寻萌 张海 王字玲 赵勇

南方医科大学学报2017,Vol.37Issue(9):1149-1155,7.
南方医科大学学报2017,Vol.37Issue(9):1149-1155,7.DOI:10.3969/j.issn.1673-4254.2017.09.02

抗恶性黑素瘤单链抗体-鱼精蛋白融合蛋白表达载体的构建及评价

Construction and verification of anti-MM scFv-tP fusion protein expression vector

王昊 1杨一飞 2王炜 3管冰 4寻萌 5张海 6王字玲 7赵勇6

作者信息

  • 1. 西安交通大学第二附属医院皮肤科,陕西西安710004
  • 2. 河北工程大学附属医院预防保健科,河北邯郸056002
  • 3. 浙江加州国际纳米技术研究院,浙江杭州310058
  • 4. 西安交通大学第一附属医院泌尿外科,陕西西安710061
  • 5. 西安交通大学基础医学院病原生物学与免疫学系,陕西西安710061
  • 6. 中国人民解放军第四军医大学实验动物中心,陕西西安710032
  • 7. 中国军事医学科学院输血研究所,北京100850
  • 折叠

摘要

Abstract

Objective To construct an expression vector of anti-MM scFv-tP fusion protein and test its expression efficiency and function.Methods The truncated protamine (tP) gene sequence was added to the gene of single chain antibody against the specific antigen on the surface of malignant melanoma tumor cells using PCR.A GST-fusion expression vector was constructed and the soluable protein was expressed in the E.coli system.After cleavage and purification,the purified fusion protein was obtained.The binding activity of Anti-MM scFv-tP and siRNA was detected by EMSA.Flow cytometry and confocal microscopy were used to detect the cell surface antigen binding activity of the fusion protein.Results The expression vector of Anti-MM scFv-tP fusion protein was successfully constructed.The soluable protein could be expressed in the E.coli system,and the purified fusion protein was obtained.The anti-MM scFv-tP fusion protein retained siRNA binding ability and could directly target malignant melanoma (MM) LiBr cells.Conclusion The recombinant GST-Anti-MM-scFv-tp expression vector was successfully constructed.The fusion protein retains siRNA binding ability and can directly target LiBr cells to provide a reliable tool for further study.

关键词

恶性黑色素瘤/单链抗体/表达载体/Anti-MM-scFv-tp

Key words

malignant melanoma/single-chain antibody/expression vector/Anti-MM-scFv-tp

引用本文复制引用

王昊,杨一飞,王炜,管冰,寻萌,张海,王字玲,赵勇..抗恶性黑素瘤单链抗体-鱼精蛋白融合蛋白表达载体的构建及评价[J].南方医科大学学报,2017,37(9):1149-1155,7.

基金项目

国家自然科学基金(30960349)Supported by National Natural Science Foundation of China (30960349). (30960349)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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