Benzel I, Weise F, Wiese M
Max-Planck-Institut für Biologie, Abteilung Membranbiochemie, Corrensstrasse 38, D-72076 Tübingen, Germany.
Mol Biochem Parasitol. 2000 Nov;111(1):77-86. doi: 10.1016/s0166-6851(00)00306-6.
The membrane-bound acid phosphatase of Leishmania mexicana (LmxMBAP) has been shown to be a heterogeneously N-glycosylated type I transmembrane protein, which is localized predominantly in vesicular structures close to the flagellar pocket in promastigotes and amastigotes. Its expression in both life stages prompted us to analyse its function by performing deletion analysis. Both alleles of the single copy gene were sequentially replaced by resistance marker genes and the resulting deletion mutant was tested for its potential to infect Balb/c mice and peritoneal macrophages. There was no obvious difference detectable between the mutant and the wild-type. Therefore, we conclude that LmxMBAP is neither involved in the infection process nor required for amastigote survival in the infected host cell. LmxMBAP null mutant promastigotes were used to establish a system for homogeneous overexpression of LmxMBAP which will be useful to investigate protein sorting in L. mexicana.
墨西哥利什曼原虫的膜结合酸性磷酸酶(LmxMBAP)已被证明是一种异质性N-糖基化的I型跨膜蛋白,主要定位于前鞭毛体和无鞭毛体中靠近鞭毛袋的囊泡结构中。它在两个生活阶段的表达促使我们通过进行缺失分析来分析其功能。单拷贝基因的两个等位基因依次被抗性标记基因取代,并对所得的缺失突变体感染Balb/c小鼠和腹膜巨噬细胞的潜力进行了测试。突变体和野生型之间没有明显的差异。因此,我们得出结论,LmxMBAP既不参与感染过程,也不是被感染宿主细胞中无鞭毛体存活所必需的。LmxMBAP基因敲除突变体前鞭毛体被用于建立一个LmxMBAP均匀过表达的系统,这将有助于研究墨西哥利什曼原虫中的蛋白质分选。