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作 者:丘玉昌[1] 朱正光[1] 徐继红[1] 徐伟[1] 吴曙光[1]
机构地区:[1]第一军医大学药物研究所,广东广州510515
出 处:《第一军医大学学报》2001年第5期332-333,共2页Journal of First Military Medical University
基 金:军队"九五"重点课题基金!(962025)
摘 要:目的对重组人肝细胞生长因子(Recombinant human hepatocyte growth facor, rhHGF)进行初步纯化及鉴定。方法 培养上清液经过离心、超滤,在FPLC系统上经肝素亲和层析分离纯化,用ELISA法检测、收集rhHGF。SDS-PAGE电 泳鉴定纯度和相对分子质量,大鼠原代肝细胞培养法检测rhHGF的生物学活性。结果rhHGF主要在0.9~1.3 mol/L NaCl 范围内被洗脱,由约62 000和34 000两个亚基组成,明显促进大鼠肝细胞DNA合成。结论 经肝素亲和层析分离,从 表达山HGF的CHO细胞培养上清液中纯化出有活性的rhHGF。Objective: To purify. and identify recombinant human hepatocyte growth facor (rhHGF) from the culture supernatant of CHO cells. Methods Affinity chromatography employing Heparin-Sepharose CL-6B column was performed to fractionate culture supernatant of CHO cells, and the fractions containing rhHGF were screened by ELISA. SDS-PAGE gel electrophoresis and the measurement of 3H-thymidine incorporation into primary culturerat hepatocytes were employed to identify rhHGF. Results The rhHGF was eluted when the concentration of NaCl was between 0.9 and l.3 mol/L. Purified rhHGF, which presented 2 bands on reduced SDS-PAGE (at 62 000 and 34 000, respectively), increased the 3H-thymidine incorporation into primary cultured rat hepatocytes. Conclusion Bioactive rhHGF can be purified by heparin affinity chromatography from the culture supernatant of CHO cells expressing rhHGF.
关 键 词:重组人肝细胞生长因子 纯化 鉴定 rhHGF
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