Department of Molecular Cell Biology and Biochemistry, Basic Veterinary Medicine, Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima, 890-0065, Japan.
Transboundary Animal Diseases Research Center, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima, 890-0065, Japan.
Histochem Cell Biol. 2019 Nov;152(5):365-375. doi: 10.1007/s00418-019-01814-3. Epub 2019 Sep 21.
Glycosylphosphatidylinositol (GPI)-anchored proteins typically localise to lipid rafts. GPI-anchored protein microdomains may be present in the plasma membrane; however, they have been studied using heterogeneously expressed GPI-anchored proteins, and the two-dimensional distributions of endogenous molecules in the plasma membrane are difficult to determine at the nanometre scale. Here, we used immunoelectron microscopy using a quick-freezing and freeze-fracture labelling (QF-FRL) method to examine the distribution of the endogenous GPI-anchored protein SAG1 in Toxoplasma gondii at the nanoscale. QF-FRL physically immobilised molecules in situ, minimising the possibility of artefactual perturbation. SAG1 labelling was observed in the exoplasmic, but not cytoplasmic, leaflets of T. gondii plasma membrane, whereas none was detected in any leaflet of the inner membrane complex. Point pattern analysis of SAG1 immunogold labelling revealed mostly random distribution in T. gondii plasma membrane. The present method obtains information on the molecular distribution of natively expressed GPI-anchored proteins and demonstrates that SAG1 in T. gondii does not form significant microdomains in the plasma membrane.
糖基磷脂酰肌醇(GPI)锚定蛋白通常定位于脂筏中。GPI-锚定蛋白微区可能存在于质膜中;然而,它们是使用异源表达的 GPI-锚定蛋白进行研究的,并且内源性分子在质膜中的二维分布在纳米尺度上很难确定。在这里,我们使用快速冷冻和冷冻断裂标记(QF-FRL)方法的免疫电子显微镜检查了内源性 GPI-锚定蛋白 SAG1 在刚地弓形虫中的纳米尺度分布。QF-FRL 原位物理固定分子,最大限度地减少人为干扰的可能性。SAG1 标记仅在弓形虫质膜的外质叶而非细胞质叶中观察到,而在内膜复合物的任何叶中均未检测到。SAG1 免疫金标记的点模式分析显示,在弓形虫质膜中主要呈随机分布。本方法可获得天然表达的 GPI-锚定蛋白的分子分布信息,并表明 SAG1 不在弓形虫质膜中形成显著的微区。