Peters Reiner
Institute of Medical Physics and Biophysics and Center for Nanotechnology, University of Münster, Germany.
Methods Mol Biol. 2006;322:259-72. doi: 10.1007/978-1-59745-000-3_18.
In this chapter, two techniques for the analysis of transport through the nuclear pore complex are described. In the first technique, nuclei isolated manually from Xenopus laevis oocytes are used to measure the import kinetics of fluorescent substrates by confocal fluorescence microscopy. In the second technique, referred to as optical single transporter recording (OSTR), isolated Xenopus oocyte nuclei, perforated nuclei, or isolated nuclear envelopes are tightly bound to planar transparent substrates containing arrays of nanoscopic-to-microscopic cavities. Transport through membrane patches spanning these cavities is recorded by confocal microscopy. By these means, the transport through single nuclear pore complexes or populations of pore complexes can be quantitatively measured.
在本章中,描述了两种分析通过核孔复合体运输的技术。在第一种技术中,使用从非洲爪蟾卵母细胞中手动分离的细胞核,通过共聚焦荧光显微镜测量荧光底物的输入动力学。在第二种技术中,称为光学单转运体记录(OSTR),将分离的非洲爪蟾卵母细胞核、穿孔核或分离的核膜紧密结合到含有纳米级到微米级腔阵列的平面透明底物上。通过共聚焦显微镜记录跨这些腔的膜片的运输。通过这些方法,可以定量测量通过单个核孔复合体或孔复合体群体的运输。