Coppi Alida, Pinzon-Ortiz Consuelo, Hutter Christina, Sinnis Photini
Department of Medical and Molecular Parasitology, New York University School of Medicine, New York, NY 10010, USA.
J Exp Med. 2005 Jan 3;201(1):27-33. doi: 10.1084/jem.20040989.
The circumsporozoite protein (CSP) is the major surface protein of Plasmodium sporozoites, the infective stage of malaria. Although CSP has been extensively studied as a malaria vaccine candidate, little is known about its structure. Here, we show that CSP is proteolytically cleaved by a papain family cysteine protease of parasite origin. Our data suggest that the highly conserved region I, found just before the repeat region, contains the cleavage site. Cleavage occurs on the sporozoite surface when parasites contact target cells. Inhibitors of CSP processing inhibit cell invasion in vitro, and treatment of mice with E-64, a highly specific cysteine protease inhibitor, completely inhibits sporozoite infectivity in vivo.
环子孢子蛋白(CSP)是疟原虫子孢子(疟疾的感染阶段)的主要表面蛋白。尽管CSP作为疟疾疫苗候选物已被广泛研究,但其结构仍知之甚少。在此,我们表明CSP被源自寄生虫的木瓜蛋白酶家族半胱氨酸蛋白酶进行蛋白水解切割。我们的数据表明,在重复区域之前发现的高度保守的区域I包含切割位点。当寄生虫接触靶细胞时,切割发生在子孢子表面。CSP加工抑制剂在体外抑制细胞侵袭,用高度特异性的半胱氨酸蛋白酶抑制剂E-64治疗小鼠可在体内完全抑制子孢子的感染性。