Wahlgren M, Aslund L, Franzén L, Sundvall M, Wåhlin B, Berzins K, McNicol L A, Björkman A, Wigzell H, Perlmann P
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2677-81. doi: 10.1073/pnas.83.8.2677.
A genomic DNA fragment that encodes a Plasmodium falciparum antigen has been isolated by using human antibodies eluted from the membrane of infected erythrocytes. The antigen has a very unusual primary structure; it is exceptionally rich in asparagine residues, many of which are distributed in clusters (2-15 residues) along the polypeptide chain. Unlike many P. falciparum antigens, this protein lacks tandemly repeated sequences. The antigen is distinct from Pf 155, a merozoite-derived antigen deposited in the membrane of infected erythrocytes, but contains epitopes that crossreact with anti-Pf 155 antibodies. Antisera prepared in mice against the asparagine-rich protein react with late-stage parasites in indirect immunofluorescence. In an in vitro merozoite reinvasion assay, the IgG fraction of a mouse polyclonal antiserum, as well as a mouse monoclonal antibody, gave significant inhibition. Three polypeptides (Mr 36,000, 30,000, and 15,000) were recognized by these antibodies on immunoblots of P. falciparum extracts.
利用从感染红细胞膜上洗脱的人源抗体,已分离出一段编码恶性疟原虫抗原的基因组DNA片段。该抗原具有非常独特的一级结构;它富含天冬酰胺残基,其中许多沿着多肽链以簇状(2 - 15个残基)分布。与许多恶性疟原虫抗原不同,这种蛋白质缺乏串联重复序列。该抗原与Pf 155不同,Pf 155是一种沉积在感染红细胞膜上的裂殖子来源抗原,但含有与抗Pf 155抗体发生交叉反应的表位。用富含天冬酰胺的蛋白质免疫小鼠制备的抗血清在间接免疫荧光中与晚期寄生虫发生反应。在体外裂殖子再入侵试验中,小鼠多克隆抗血清的IgG组分以及一种小鼠单克隆抗体都产生了显著的抑制作用。在恶性疟原虫提取物的免疫印迹上,这些抗体识别出三种多肽(分子量分别为36,000、30,000和15,000)。