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作 者:郭建巍[1] 冯健男[2] 马骢[1] 扬霄鹏[3] 沈倍奋[2]
机构地区:[1]海军总医院检验科,北京100037 [2]军事医学科学院基础医学研究所分子免疫学实验室,北京100850 [3]兰州军区兰州总医院医学实验中心,甘肃兰州730050
出 处:《第四军医大学学报》2007年第14期1275-1278,共4页Journal of the Fourth Military Medical University
基 金:国家高技术研究发展计划(863)(2002AA232021和2004AA002020);中国博士后基金(2004035289)
摘 要:目的:实现基于中和性单抗4C13单链抗体的真核表达,并对其生物学活性进行评价.方法:用TRIzol提取抗ricin中和性单抗杂交瘤细胞4C13总RNA,扩增其轻、重链可变区基因,登陆GenBank;用Linker(GGGGS)3将VH和VL连接,用重叠延伸PCR克隆入真核表达载体pCDNA3.1,用脂质体转染293T细胞,对瞬时表达产物进行生物学活性检测.结果:中和性单抗杂交瘤细胞4C13轻、重链可变区基因在GenBank中的登录号为DQ389248和DQ389245,ScFv与ricin可特异性结合,培养上清原液和2倍稀释液的抑制率分别为33.7%和29%;ScFv在ricin浓度为0.01~0.005ng/mL时可中和ricin对SP2/0细胞的细胞毒,随着ricin浓度逐渐增大,细胞存活率逐渐减低.结论:研究结果为研制基于中和性单抗的其他ricin拮抗剂奠定了重要的理论和实践基础.AIM : To realize an anti-ricin neutralizing monoclonal antibody-based ScFv proteins with high biological activity in the pCDNA3. 1 vector expression system and to evaluate the neutralizing activities of ScFv. METHODS: The total RNA was obtained by TRIzol from an anti-ficin neutralizing monoclonal anti- body hybridoma cell named 4C13 and heavy-chain and light-chain variable fragments (VH, VL) were amplified by overlap PCR and accepted by Genbank of NCBI. V. and VL were linked by (GGGGS)3 with a direction of VH-linker-VL and cloned to pCDNA3.1 vector expression system. The biological activities of ScFv obtained from 293T cell culture fluids infected by liposome were evaluated. RESULTS: The accession number of VH and VL genes of anti-ricin neutralizing monoclonal antibody was DQ389248 and DQ389245. ScFv could bind with ricin specifically. Inhibition percentage of culture liquid of 293T cell without dilution and with 2 times dilution was 33.7% and 29%, respectively. ScFv could neutralize the cytotoxic effects of ricin to SP2/0 cells at the concentration of 0.01 -0. 005 ng/mL in a nice dose-effect relation. CONCLUSION: The nice biological activi- ties of ScFv have established an important basement for further study of other anti-ricin neutralizing monoclonal antibody-based antidotes.
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