Coppel R L, Brown G V, Mitchell G F, Anders R F, Kemp D J
EMBO J. 1984 Feb;3(2):403-7. doi: 10.1002/j.1460-2075.1984.tb01820.x.
A cDNA library was constructed in pBR322 using mRNA from blood stages of a Papua New Guinean isolate of Plasmodium falciparum. Expression of parasite antigens was not directly detectable by conventional immunological assays. To circumvent this, mice were immunized with lysates of cDNA clones, and the antisera raised were assayed for anti-parasite reactivity. One cDNA clone was identified which reliably elicited antibodies to P. falciparum. The mouse antisera were used to characterize the native P. falciparum protein as a 120-kd protein, which is antigenic during natural infection. The protein occurs in late trophozoite and schizont stages and is found in isolates of the parasite from widely separated geographical areas. The genomic context of the antigen gene is conserved in the different isolates.
使用来自巴布亚新几内亚恶性疟原虫分离株血液阶段的mRNA构建了一个pBR322载体的cDNA文库。传统免疫分析无法直接检测到寄生虫抗原的表达。为了克服这一问题,用cDNA克隆的裂解物免疫小鼠,并检测产生的抗血清的抗寄生虫反应性。鉴定出一个能可靠地引发针对恶性疟原虫抗体的cDNA克隆。小鼠抗血清用于将天然恶性疟原虫蛋白鉴定为一种120kd的蛋白,该蛋白在自然感染期间具有抗原性。该蛋白出现在滋养体后期和裂殖体阶段,并且在来自广泛分离地理区域的寄生虫分离株中也有发现。抗原基因的基因组背景在不同分离株中是保守的。