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作 者:袁芳艳[1] 何玉龙[1] 赵娜[1] 聂芬[1] 伍晓雄[2] 龙良启[2] 李奎[3] 罗晓松[4]
机构地区:[1]华中农业大学水产学院,武汉430070 [2]华中农业大学动物医学院,武汉430070 [3]中国农业科学院畜牧研究所,北京100094 [4]中国水产科学研究院长江水产研究所,荆州434000
出 处:《华中农业大学学报》2006年第6期591-594,共4页Journal of Huazhong Agricultural University
基 金:国家"863"项目(2001AA222241)资助
摘 要:用生长抑素(somatostatin,SS)疫苗“激生1号”免疫日本大耳兔得到抗血清,经饱和硫酸铵粗提IgG,再经DEAE-sephadex-A50低压层析系统纯化后,以此IgG作为筛选配基,对随机十二肽库进行4轮淘洗。随机挑取22个噬菌斑进行双夹心ELISA,结果有6个克隆与SS抗体有较强的特异性结合力,竞争抑制ELISA进一步证明6个克隆有较好的抑制作用。将6个阳性克隆提取ssDNA进行测序,测序结果中有5个克隆的外源肽序列完全一致,经与SS氨基酸序列比对,发现两者有共同序列FWK,说明5个克隆模拟了生长抑素的抗原表位。The sera were obtained by immunizing the rabbit with somatostatin vaccine. The 1gG rudely purified by saturated ammonia sulphate was purified through DEAE-sephadex-A50 low pressure chromatography system. Using the IgG as target,a 12-mer random peptide library was biopanned for 4 rounds. The 22 clones eluted from 4rd panning were picked out randomly and characterized. Six positive clones among 22 clones were identifited by sandwith ELISA and competition ELISA. The ssDNA of the 6 positive clones were abstracted and sequenced . The results showed that five clones had the same sequence. Compared with SS amino acid sequence, the FWK was their homogerous.
分 类 号:S852.5[农业科学—基础兽医学]
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