Cheung A, Shaw A R, Leban J, Perrin L H
EMBO J. 1985 Apr;4(4):1007-11. doi: 10.1002/j.1460-2075.1985.tb03731.x.
A complementary DNA library was constructed from mRNA purified from asexual blood forms of Plasmodium falciparum. Among the members of this library we have identified a plasmid (pMC31-1) coding for a polypeptide exposed at the surface of merozoites, the invasive stage of the asexual cycle. This plasmid was identified by direct expression using both polyclonal and monoclonal antibodies specific for a schizont polypeptide of 200 kd which has been shown to be processed to an 83-kd polypeptide expressed at the surface of merozoites. The cDNA portion of the pMC31-1 plasmid hybridizes with DNA from three isolates of P. falciparum. Antisera raised against extracts of Escherichia coli harbouring pMC31-1 react with surface and internal structures of schizonts and with the surface of merozoites from all the isolates of P. falciparum examined. These results suggest that plasmid pMC31-1 encodes an antigen of value for the development of a vaccine against malaria.
从恶性疟原虫无性血液阶段纯化的mRNA构建了一个互补DNA文库。在该文库成员中,我们鉴定出一个编码裂殖子表面暴露多肽的质粒(pMC31 - 1),裂殖子是无性周期的侵入阶段。该质粒是通过直接表达鉴定的,使用了针对200kd裂殖体多肽的多克隆和单克隆抗体,该多肽已被证明可加工成在裂殖子表面表达的83kd多肽。pMC31 - 1质粒的cDNA部分与来自三个恶性疟原虫分离株的DNA杂交。针对携带pMC31 - 1的大肠杆菌提取物产生的抗血清与裂殖体的表面和内部结构以及所有检测的恶性疟原虫分离株的裂殖子表面发生反应。这些结果表明,质粒pMC31 - 1编码一种对疟疾疫苗开发有价值的抗原。