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首页> 外文期刊>Microscopy >Analysis of the complexity of the sperm acrosomal membrane by super-resolution stimulated emission depletion microscopy compared with transmission electron microscopy.
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Analysis of the complexity of the sperm acrosomal membrane by super-resolution stimulated emission depletion microscopy compared with transmission electron microscopy.

机译:与透射电子显微镜相比,通过超高分辨率激发发射耗尽显微镜分析精子顶体膜的复杂性。

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摘要

The acrosome is a Golgi-derived sperm cell organelle enclosed by a continuous acrosomal membrane. The acrosomal membrane complexes with surrounding matrices containing molecules necessary for fertilization; however, the complex of acrosomal membrane and associating matrices (CAMAM) has not been visualized in detail under living conditions. Here, we analyzed the CAMAM at the nanometer level using super-resolution stimulated emission depletion (STED) fluorescence microscopy and equatorin-enhanced green fluorescent protein transgenic mice. The STED images were compared with the corresponding images taken by immunoelectron microscopy. Consequently, the substructure of CAMAM could be differentiated at nanometer-scale resolution by STED microscopy without the need for sectioning. The information obtained in this study will be beneficial not only for understanding the molecular mechanism of fertilization but also for cell imaging under living conditions.
机译:顶体是被连续的顶体膜包围的高尔基体来源的精子细胞器。顶体膜与周围基质复合,其中包含受精所需的分子;但是,顶体膜和缔合基质(CAMAM)的复合体在生活条件下并未详细显示。在这里,我们使用超高分辨率激发发射耗尽(STED)荧光显微镜和赤道素增强型绿色荧光蛋白转基因小鼠在纳米水平上分析了CAMAM。将STED图像与通过免疫电子显微镜拍摄的相应图像进行比较。因此,CAMAM的亚结构可以通过STED显微镜在纳米级分辨率下进行区分,而无需进行切片。在这项研究中获得的信息将不仅有助于了解受精的分子机制,而且对于生活条件下的细胞成像也将是有益的。

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