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Disrupting assembly of the inner membrane complex blocks Plasmodium falciparum sexual stage development

机译:破坏内膜复合物的组装阻碍恶性疟原虫性阶段的发展

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摘要

Transmission of malaria parasites relies on the formation of a specialized blood form called the gametocyte. Gametocytes of the human pathogen, Plasmodium falciparum, adopt a crescent shape. Their dramatic morphogenesis is driven by the assembly of a network of microtubules and an underpinning inner membrane complex (IMC). Using super-resolution optical and electron microscopies we define the ultrastructure of the IMC at different stages of gametocyte development. We characterize two new proteins of the gametocyte IMC, called PhIL1 and PIP1. Genetic disruption of PhIL1 or PIP1 ablates elongation and prevents formation of transmission-ready mature gametocytes. The maturation defect is accompanied by failure to form an enveloping IMC and a marked swelling of the digestive vacuole, suggesting PhIL1 and PIP1 are required for correct membrane trafficking. Using immunoprecipitation and mass spectrometry we reveal that PhIL1 interacts with known and new components of the gametocyte IMC.
机译:疟疾寄生虫的传播依赖于一种称为配子体细胞的特殊血液形式的形成。人类病原体恶性疟原虫的配子细胞呈月牙形。它们惊人的形态发生是由微管网络和基础内膜复合物(IMC)的组装驱动的。使用超高分辨率光学和电子显微镜,我们定义了配子细胞发育不同阶段的IMC超微结构。我们表征了配子细胞IMC的两个新蛋白,称为PhIL1和PIP1。 PhIL1或PIP1的遗传破坏消除了伸长,并阻止了可传播的成熟配子细胞的形成。成熟缺陷伴随着不能形成包膜的IMC和消化液泡的明显肿胀,表明PhIL1和PIP1是正确的膜运输所必需的。使用免疫沉淀和质谱,我们揭示了PhIL1与配子细胞IMC的已知和新成分相互作用。

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