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作 者:李伊培[1,2] 高丽华[2] 张连成[2] 邵勇[2] 刘羽[2] 潘芸[3] 高招刚[3] 张嵘[1] 胡显文[2] 陈惠鹏[2]
机构地区:[1]沈阳药科大学生命科学与生物制药学院,辽宁沈阳110016 [2]军事医学科学院生物工程研究所,北京100071 [3]安徽大学生命科学学院,安徽合肥230601
出 处:《生物技术通讯》2014年第2期165-169,共5页Letters in Biotechnology
基 金:国家自然科学基金(30973670;81202445)
摘 要:目的:表达优化的血管内皮细胞生长因子(VEGF)受体1(VEGFR1)胞外区第2个类免疫球蛋白结构域(VEGFR1D2)和VEGF受体2(VEGFR2)胞外区第3个类免疫球蛋白结构域(VEGFR2D3)与人IgG1 Fc片段的融合产物VEGF-Trap2,探讨该产物与人源VEGF165(hVEGF165)之间的亲和力。方法:将优化的目的基因VEGFR1D2/R2D3连接到真核表达载体pIRES2-EGFP-Fc中,转染CHO-K1细胞并筛选高表达目的蛋白VEGF-Trap2的细胞系,亲和纯化VEGF-Trap2蛋白,通过非竞争性ELISA及生物膜干涉技术检测VEGF-Trap2与hVEGF165之间的亲和力。结果:DNA测序表明真核表达载体pIRES2-EGFP-VEGF-Trap2序列正确;获得表达VEGF-Trap2的细胞系;非竞争性ELISA实验中,VEGF-Trap2与hVEGF165功能性亲和常数达到1.86×107L/mol;生物膜干涉实验中,hVEGF165与VEGF-Trap2的平衡解离常数达到3.13×10-9mol/L。结论:构建了真核表达载体pIRES2-EGFP-VEGF-Trap2并在CHO-K1细胞中稳定表达,重组蛋白VEGF-Trap2与hVEGF165有较高的亲和力,提示其可用于阻断VEGF信号传导途径,为该蛋白进一步的体外及体内实验奠定了基础。Objective: To investigate affinity between human VEGF165(hVEGFt65) and the expressed product of optimized the second immunoglobulin(Ig) domain of VEGFRI(VEGFR1D2) and the third Ig domain of VEGFR2 (VEGFR2D3) fused to human IgG1. Methods: The optimized VEGFRID2/R2D3 gene was cloned into eukaryotie expression vector plRES2-EGFP-Fc, and then the construct named as plRES2-EGFP-VEGF-Trap2 was transfect ed into CHO-K1 cells and screened with antibiotics G418. Protein VEGF-Trap2 was purified by affinity chromatog raphy and the affinity between VEGF-Trap2 with hVEGF165 was evaluated through non-competitive ELISA and bio layer interferometry. Results: DNA sequencing proved that the sequence of eukaryotic expression vector plRES2- EGFP-VEGF-Trap2 was correct, and the CHO-K1 cell line expressing VEGF-Trap2 was got. The functional affini- ty of VEGF-Trap2 1.86×10^7 L/mol was determined by non-competitive ELISA, and the equilibrium dissociation constant of VEGF-Trap2 for hVEGF165 3.13x10^-9 mol/L was analyzed by biolayer interferometry. Conclusion: Re combinant protein VEGF-Trap2 has high affinity with hVEGF165, which suggests that VEGF-Trap2 can be used to block VEGF signaling pathway and provides basis for further study in vitro and in vivo.
关 键 词:血管内皮细胞生长因子受体 VEGF-Trap FC融合蛋白 CHO-K1细胞 抗肿瘤
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