National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Malaria, Schistosomiasis and Filariasis, Key Laboratory of Parasite and Vector Biology Ministry of Health, Shanghai 200025, People's Republic of China.
J Proteomics. 2013 Jan 14;78:148-58. doi: 10.1016/j.jprot.2012.11.020. Epub 2012 Nov 29.
With the completion of the functional genome, merozoite proteome and stage-specific transcriptomes of the intraerythrocytic developmental cycle of Plasmoidum falciparum, the development of new vaccine candidates targeting Plasmodium merozoites is now possible. Here we report using protein array technology to detect antibody responses to Plasmodium merozoite proteins by screening the serum of Plasmodium-exposed individuals. A total of 138 genes encoding P. falciparum merozoite proteins were cloned using the In-Fusion cloning method and expressed using a wheat germ cell-free system (WGCF). These proteins were then screened with serum from Plasmodium-exposed individuals and unexposed subjects using protein arrays. A total of 30 highly immunoreactive merozoite antigens were identified (21.7% of 138 target proteins), including 10 well-characterized blood-stage vaccine candidates for P. falciparum. In addition, we report for the first time 7 proteins (MSP3.5, MRSP2, ETRAMP11.2, ETRAMP14.1 and RALP1, and two hypothetical proteins PFA0210c and PF14_0572) as being immunologically reactive. These novel Plasmodium merozoite antigens may be potential vaccine candidates for blood-stage malaria, and warrant further study.
随着恶性疟原虫(Plasmodium falciparum)红内期发育周期的功能基因组、裂殖子蛋白组和阶段特异性转录组的完成,针对疟原虫裂殖子的新型疫苗候选物的开发成为可能。在此,我们报告了使用蛋白质芯片技术通过筛选疟原虫暴露个体的血清来检测针对疟原虫裂殖子蛋白的抗体反应。使用 In-Fusion 克隆方法克隆了编码恶性疟原虫裂殖子蛋白的 138 个基因,并使用小麦胚细胞无细胞系统(WGCF)进行表达。然后使用蛋白质芯片筛选疟原虫暴露个体和未暴露个体的血清。共鉴定出 30 种高度免疫反应性的裂殖子抗原(占 138 个靶蛋白的 21.7%),其中包括 10 种恶性疟原虫成熟的血期疫苗候选物。此外,我们首次报道了 7 种蛋白(MSP3.5、MRSP2、ETRAMP11.2、ETRAMP14.1 和 RALP1,以及两个假定蛋白 PFA0210c 和 PF14_0572)具有免疫反应性。这些新型疟原虫裂殖子抗原可能是血期疟疾的潜在疫苗候选物,值得进一步研究。