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作 者:马艳[1] 李伟[2] 李小波[1] 鲍冬梅[1] 卢建培
机构地区:[1]广东药科大学基础学院广东省生物活性药物研究重点实验室,广东广州510006 [2]广东药科大学中药学院,广东广州510006
出 处:《生物工程学报》2016年第12期1715-1726,共12页Chinese Journal of Biotechnology
基 金:国家自然科学基金(No.81502520);广东省自然科学基金(No.2016A030310299)资助~~
摘 要:为了获得足够多纯度高且有活性的肝靶向肽-人内皮抑制素融合蛋白(HTP-r ES),首先研究了BL21/p ET21b-HTP-r ES重组菌株的生长曲线和最佳诱导时机;单因素分析不同p H值、不同诱导时间、不同诱导剂浓度、不同诱导温度时融合蛋白表达量;通过包涵体洗涤、复性、纯化,以获得高纯度的肝靶向肽-人内皮抑制素融合蛋白;最后采用流式细胞仪和MTT对融合蛋白进行活性鉴定。结果表明,BL21/p ET21b-HTP-r ES重组菌株在1.5–3.5 h处于对数生长期,培养基p H 8.0、IPTG终浓度0.06 mmol/L、42℃、诱导表达5 h为最佳表达条件。包涵体洗涤后纯度达60%,经复性、纯化后获得的目的蛋白纯度达到95%以上,对人肝癌细胞具有靶向性,能抑制人脐静脉内皮细胞的增殖。研究确立了融合蛋白最佳表达条件以及复性、纯化条件,为进一步研究其生物学活性及药物开发奠定基础。To obtain sufficient purified and active fusion protein-hepatocyte-targeting peptide-human endostatin(HTP-r ES),we studied the growth curve and the optimal induction timing of BL21/p ET21b-HTP-r ES.Different conditions of p H value,induction time,induction concentration and induction temperature were optimized by univariate analysis.After washing,refolding and purifying,the activity of fusion protein was identified by flow cytometry and 3-(4,5)-dimethylthiahiazo(-z-y1)-3,5-di-phenytetrazoliumromide(MTT).Results show that the logarithmic growth phase of BL21/p ET21b-HTP-r ES was from 1.5 h to 3.5 h,the optimum expression conditions were p H 8.0,0.06 mmol/L IPTG,at 42 for 5 h.The purity of ℃inclusion bodies was up to 60% after washing.The purity of target protein was more than 95% after refolding and purification.Our findings provide the foundation for further biological activity and drug development.
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