Imaging Yeast NPCs: From Classical Electron Microscopy to lmmuno-SEM

被引:1
|
作者
Kiseleva, Elena [1 ]
Richardson, A. Christine [2 ]
Fiserova, Jindriska [2 ]
Strunov, Anton A. [1 ]
Spink, Matthew C. [2 ]
Johnson, Simeon R. [2 ]
Goldberg, Martin W. [2 ]
机构
[1] Russian Acad Sci, Inst Cytol & Genet, Lab Morphol & Funct Cell Struct, Novosibirsk 630090, Russia
[2] Univ Durham, Dept Biol & Biomed Sci, Durham, England
基金
英国生物技术与生命科学研究理事会;
关键词
NUCLEAR-PORE COMPLEX; SACCHAROMYCES-CEREVISIAE; RNA TRANSPORT; ENVELOPE; VISUALIZATION; RESOLUTION; FILAMENTS; PROTOCOL; PROTEIN;
D O I
10.1016/B978-0-12-417160-2.00003-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Electron microscopy (EM) has been used extensively for the study of nuclear transport as well as the structure of the nuclear pore complex (NPC) and nuclear envelope. However, there are specific challenges faced when carrying out EM in one of the main model organisms used: the yeast, Saccharomyces cerevisiae. These are due to the presence of a cell wall, vacuoles, and a densely packed cytoplasm which, for transmission EM (TEM), make fixation, embedding, and imaging difficult. These also present problems for scanning EM (SEM) because cell wall removal and isolation of nuclei can easily damage the relatively fragile NPCs. We present some of the protocols we use to prepare samples for TEM and SEM to provide information about yeast NPC ultrastructure and the location of nucleoporins and transport factors by immunogold labeling within that ultrastructure.
引用
收藏
页码:59 / 79
页数:21
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