Sullivan D J, Gluzman I Y, Goldberg D E
Howard Hughes Medical Institute, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Science. 1996 Jan 12;271(5246):219-22. doi: 10.1126/science.271.5246.219.
The digestive vacuole of Plasmodium falciparum is the site of hemoglobin degradation, heme polymerization into crystalline hemozoin, and antimalarial drug accumulation. Antibodies identified histidine-rich protein II (HRP II) in purified digestive vacuoles. Recombinant or native HRP II promoted the formation of hemozoin, and chloroquine inhibited the reaction. The related HRP III also polymerized heme, and an additional HRP was identified in vacuoles. It is proposed that after secretion by the parasite into the host erythrocyte cytosol, HRPs are brought into the acidic digestive vacuole along with hemoglobin. After hemoglobin proteolysis, HRPs bind the liberated heme and mediate hemozoin formation.
恶性疟原虫的消化泡是血红蛋白降解、血红素聚合成结晶状疟色素以及抗疟药物积累的场所。抗体在纯化的消化泡中鉴定出富含组氨酸的蛋白II(HRP II)。重组或天然的HRP II促进疟色素的形成,而氯喹抑制该反应。相关的HRP III也能使血红素聚合,并且在泡中鉴定出另一种HRP。有人提出,寄生虫分泌到宿主红细胞胞质溶胶后,HRP与血红蛋白一起被带入酸性消化泡。血红蛋白被蛋白水解后,HRP结合释放出的血红素并介导疟色素的形成。