首页> 外文会议>Conference on Laser Microscopy, Jul 7-8, 2000, Amsterdam, Netherlands >Single molecule fluorescence microscopy on Nucleotide Excision Repair complexes using GFP fusion proteins
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Single molecule fluorescence microscopy on Nucleotide Excision Repair complexes using GFP fusion proteins

机译:使用GFP融合蛋白对核苷酸切除修复复合物进行单分子荧光显微镜检查

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Scanning Confocal Fluorescence Microscopy is used for single molecule studies on DNA-protein complexes that occur in Nucleotide Excision Repair (NER). During DNA-damage elimination by the NER-pathway, complex protein structures assemble over DNA. It is our aim to resolve the architecture of these DNA-protein complexes and to study dynamic changes that occur in these structures. For this purpose NER-complexes are partly reconstituted onto DNA-substrates using NER-proteins fused to different Green Fluorescent Protein (GFP) mutants. Here we describe the recombinant production of NER-GFP fusion proteins. Characterization of GFP fluorescence is shown together with results of GFP single molecule imaging. First results with NER-GFP fusion proteins are presented as well.
机译:扫描共聚焦荧光显微镜用于核苷酸切除修复(NER)中发生的DNA-蛋白质复合物的单分子研究。在通过NER途径消除DNA损伤的过程中,复杂的蛋白质结构在DNA上组装。我们的目标是解决这些DNA-蛋白质复合物的结构,并研究这些结构中发生的动态变化。为此,使用与不同绿色荧光蛋白(GFP)突变体融合的NER蛋白,将NER复合物部分重组到DNA底物上。在这里,我们描述了NER-GFP融合蛋白的重组生产。显示了GFP荧光的特征以及GFP单分子成像的结果。还介绍了NER-GFP融合蛋白的初步结果。

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