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人骨形态发生蛋白-2的基因重组及其在大肠杆菌中的表达
引用本文:Ma Q,Dang G,Ma D. 人骨形态发生蛋白-2的基因重组及其在大肠杆菌中的表达[J]. 中华医学杂志, 1998, 78(4): 308-310
作者姓名:Ma Q  Dang G  Ma D
作者单位:北京医科大学第三医院骨科
摘    要:目的用基因工程技术在大肠杆菌中表达人骨形态发生蛋白2(hBMP2)。方法将包含hBMP2部分前肽和成熟肽的3′端730bpcDNA片段,插入原核表达载体pkpL3a的多克隆位点,构建成pKpL3a/hBMP2重组表达载体,转化大肠杆菌pop2136,挑选阳性克隆,经诱导表达后用SDSPAGE鉴定。结果该克隆表达的hBMP2为MW27000,表达量占菌体总蛋白10%,部分纯化后植入大鼠股部肌肉,组织学观察到肌肉内大量间充质细胞增生及骨与软骨形成。结论说明重组hBMP2具有诱导异位骨与软骨形成的生物学功能。

关 键 词:基因.合成  骨结合素  大肠杆菌

Human bone morphogenetic protein-2: recombinant expression in E. coli
Ma Q,Dang G,Ma D. Human bone morphogenetic protein-2: recombinant expression in E. coli[J]. Zhonghua yi xue za zhi, 1998, 78(4): 308-310
Authors:Ma Q  Dang G  Ma D
Affiliation:Department of Orthopaedics, Third Teaching Hospital, Beijing Medical University.
Abstract:OBJECTIVE: To explore the way of producing human bone morphogenetic protein-2(hBMP-2) for bone healing by using the gene engeneering techniques. METHODS: hBMP-2 cDNA fragment, which consists of 3' end partial propeptide and mature peptide sequence, was inserted into the multiple cloning site of expression vector pkpL-3a via ligation. The recombinant plasmid pkpL-3a/hBMP-2 was transformed into E. coli pOp2136. By the method of restriction map, the positive expression clone was selected. SDS-PAGE analysis showed a new foreign protein band near 27,000 after induction. The yield of induced hBMP-2 accouned for 10% of the total bacterial proteins. RESULTS: The partial purified recombinant hBMP-2 was implanted into Wistar rat thigh. After 4 weeks, histological analysis showed that it induced the proliferation of mesenchymal type cells and formation of new cartilage and bone in the implantation area. CONCLUSION: The hBMP-2 produced by gene engeneering techniques has the biologic capacity of ectopic bone formation.
Keywords:Genes Osteonectin Escherichia coli  
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