Martinez S L, Clavijo C A, Winograd E
Laboratorio de Biología Celular, Instituto Nacional de Salud, Bogotá, Colombia.
Mol Biochem Parasitol. 1998 Mar 15;91(2):273-80. doi: 10.1016/s0166-6851(97)00206-5.
During intracellular development of the malarial parasite numerous membranous vesicles appear in the infected erythrocyte cytoplasm between the parasitophorous vacuolar membrane (PVM) and the erythrocyte plasma membrane. In this study we describe the characterization of a monoclonal antibody which recognizes two major parasite-encoded proteins of 50 and 41 kDa. Immunofluorescence and immunoelectron microscopy demonstrated that the monoclonal antibody reacts with cytoplasmic vesicles of Plasmodium falciparum infected erythrocyte referred to as Maurer's clefts. The antigens recognized by the monoclonal antibody were expressed very early during the erythrocytic life cycle of the parasite, and remained tightly associated within membrane vesicles even after merozoites are released from infected erythrocytes. The antigens were partially soluble in non-ionic detergents, and were released from the membrane by alkali treatment, indicating that the proteins recognized by the monoclonal antibody are peripheral membrane proteins. It is proposed that the 50 and 41 kDa antigens might be part of an underlying membrane skeletal network that provides structural support to vesicles and tubules present in the infected erythrocyte cytoplasm.
在疟原虫的细胞内发育过程中,许多膜性小泡出现在被感染红细胞胞质中,位于寄生泡膜(PVM)和红细胞质膜之间。在本研究中,我们描述了一种单克隆抗体的特性,该抗体可识别两种主要的由寄生虫编码的蛋白质,分子量分别为50 kDa和41 kDa。免疫荧光和免疫电子显微镜显示,该单克隆抗体与恶性疟原虫感染红细胞的胞质小泡(称为毛氏小体)发生反应。单克隆抗体识别的抗原在寄生虫的红细胞生命周期早期就已表达,即使裂殖子从感染的红细胞中释放后,仍紧密结合在膜性小泡内。这些抗原部分可溶于非离子去污剂,并可通过碱处理从膜上释放出来,这表明单克隆抗体识别的蛋白质是外周膜蛋白。有人提出,50 kDa和41 kDa的抗原可能是潜在膜骨架网络的一部分,该网络为存在于被感染红细胞胞质中的小泡和小管提供结构支持。