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恶性疟原由海南株cDNA克隆FMPf01分析 被引量:2

ANALYSIS OF cDNA CLONE (FMPf01) FROM cDNA EXPRESSION LIBRARY OF ERYTHROCYTIC STAGE PLASMODIUM FALCIPARUM (FCC/HN)
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摘要 目的对我室构建恶性疟原虫海南株(FCC/HN)红内期cDNA表达文库阳性克隆(FMPf01)进行分析研究,确定其性质。方法通过计算机软件和免疫印迹法分析FMU01的减基构成、同源性及编码多肽的免疫反应性。结果核苷酸序列分析显示其A+T构成比高于G+C,为3.14:1,与基因资料库中疟原虫基因的同源性较低,其最高值为63.8%,Westernblot分析证实其编码多肽可被抗疟原虫免疫血清识别,反应性较强。结论FMPf01编码多肽有望成为疟疾免疫学诊断和疫苗的候选抗原。 Aim To sequence and analyze a clone(FMPf01)from cDNA expression library of erythrocytic stage Plas-modium falciparum- Methods Computer programs and Western b1ot were used. Result The FMPfO1 contains high ratio ofA and T. A+T/G+C is 3. l4. The best scores of similarity to the gene sequences of Plasmodium in Gen Bank are between55. 6 % ~63' 8%. The expressed peptide of FMPfO1 reacted with serum from the rabbit immunized with P. falciParnm. Cou-clusion The FMPfO1 might be a candidate antigen for the development of malaria vaccine and immunodiagnostic methods.
出处 《中国人兽共患病杂志》 CSCD 北大核心 1999年第3期40-42,53,共4页 Chinese Journal of Zoonoses
基金 全军医药卫生基金!96L034
关键词 疟疾 恶性疟 CDNA 疟原虫 克隆 序列分析 Plasmodium falciparum cDNA clone sequencing expression
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