Laboratório de Biologia Celular, Instituto Carlos Chagas/Fiocruz, 81.350-010 Curitiba, PR, Brazil.
J Microbiol Methods. 2012 Oct;91(1):101-5. doi: 10.1016/j.mimet.2012.07.013. Epub 2012 Jul 20.
Here we describe the visualization by confocal microscopy of ingested gold (15 nm)-labeled transferrin in epimastigote forms of the protozoan Trypanosoma cruzi. Intracellular gold labeling was evident at two sites, which represent the bottom of the cytopharynx and the reservosomes. The gold tracer was best observed by confocal microscopy by using the 633 nm excitation wavelength. Intracellular gold clusters larger than 60 nm could be visualized by either gold reflection (light scattering) or photoluminescence modes. The gold reflection mode, the gold photoluminescence mode and the anti-transferrin immunofluorescence image of gold-labeled transferrin showed co-localization, thus demonstrating that the gold visualization modes did not represent artifacts or mislocalization of the biomarker. Visualization of protein-gold nanoparticle complexes by confocal microscopy thus emerges as a promising imaging tool to explore the endocytic pathway in trypanosomes and other cell types, as well as to perform immunolocalization studies using gold-labeled secondary antibodies.
在这里,我们通过共聚焦显微镜描述了摄入的金(15nm)标记转铁蛋白在原生动物克氏锥虫的前鞭毛体形式中的可视化。在两个部位可以明显看到细胞内的金标记,这两个部位代表胞咽的底部和储备体。通过使用 633nm 的激发波长,共聚焦显微镜可以最好地观察到金示踪剂。可以通过金反射(光散射)或光致发光模式来观察大于 60nm 的细胞内金簇。金反射模式、金光致发光模式和金标记转铁蛋白的抗转铁蛋白免疫荧光图像显示共定位,因此证明金可视化模式不代表生物标志物的伪影或定位错误。通过共聚焦显微镜观察蛋白质-金纳米颗粒复合物,因此成为探索锥虫和其他细胞类型的内吞途径以及使用金标记的二级抗体进行免疫定位研究的有前途的成像工具。