Kun J, Hesselbach J, Schreiber M, Scherf A, Gysin J, Mattei D, Pereira da Silva L, Müller-Hill B
Institut für Genetik Universität zu Köln, Germany.
Res Immunol. 1991 Mar-Apr;142(3):199-210. doi: 10.1016/0923-2494(91)90059-r.
Genomic DNA fragments of Plasmodium falciparum generated by mung bean nuclease digestion were cloned in the lambda expression vector lambda JK2. The resulting library was screened with a rabbit antiserum raised against purified membranes of P. falciparum-infected erythrocytes and with a serum pool from immune humans from an endemic area of Liberia. Positive clones were rescreened with a series of human and monkey sera. Twelve selected clones were analysed in detail. Four of them corresponded to already described membrane-associated P. falciparum antigens. The other positive clones contained inserts which, according to the nucleotide sequence, Southern blot analysis and immunological characteristics, correspond to so far unknown antigens.
用绿豆核酸酶消化产生的恶性疟原虫基因组DNA片段被克隆到λ表达载体λJK2中。用针对恶性疟原虫感染红细胞纯化膜产生的兔抗血清以及来自利比里亚流行地区免疫人群的血清库对所得文库进行筛选。用一系列人和猴血清对阳性克隆进行再次筛选。对12个选定的克隆进行了详细分析。其中4个对应于已描述的与膜相关的恶性疟原虫抗原。其他阳性克隆所含的插入片段,根据核苷酸序列、Southern印迹分析和免疫学特征,对应于迄今未知的抗原。