Institute for Biochemistry and Pathobiochemistry Department of Systems Biochemistry, Faculty of Medicine, Ruhr University of Bochum, Bochum, Germany.
Methods Mol Biol. 2023;2643:445-453. doi: 10.1007/978-1-0716-3048-8_32.
Insect-transmitted trypanosomatid parasite infections cause life-threatening neglected tropical diseases (NTDs), including African sleeping sickness, Chagas disease and leishmaniasis. In these parasites, glycosomes are unique organelles that are essential for the parasite survival. Proper biogenesis of glycosomes is crucial to ensure correct compartmentation of the glycosomal metabolism. Genetic or chemical disruption of the glycosome biogenesis leads to a mislocalization of the glycosomal enzymes into the cytosol, which results in toxicity to the parasites. Here, we describe a detailed protocol for biochemical fractionation of Trypanosoma brucei parasites to detect mislocalization of glycosomal proteins to the cytosol. This approach utilizes increasing concentrations of digitonin that first permeabilizes the plasma membrane, followed by permeabilization of other organelles, depending on their cholesterol content. Fractionated samples can be further analyzed using immunoblotting for specific marker proteins or quantified by the specific enzyme activities.
昆虫传播的锥体虫寄生虫感染会导致危及生命的被忽视热带病(NTDs),包括非洲昏睡病、恰加斯病和利什曼病。在这些寄生虫中,糖体是独特的细胞器,对寄生虫的生存至关重要。糖体的正确生物发生对于确保糖体代谢的正确区室化至关重要。糖体生物发生的遗传或化学破坏会导致糖体酶错误定位到细胞质中,从而导致寄生虫中毒。在这里,我们描述了一种详细的生化分离方案,用于检测布鲁氏锥虫寄生虫中糖体蛋白向细胞质的错误定位。该方法利用不同浓度的脱氧胆酸钠首先使质膜通透,然后根据胆固醇含量使其他细胞器通透。分离的样品可以进一步通过免疫印迹分析特定的标记蛋白,或通过特定的酶活性进行定量。