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Single molecule fluorescence microscopy on Nucleotide Excision Repair complexes using GFP fusion proteins

机译:使用GFP融合蛋白核苷酸切除修复复合物的单分子荧光显微镜

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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:扫描共焦荧光显微镜用于单分子研究,其在核苷酸切除修复(ner)中发生的DNA-蛋白复合物。在通过途径的DNA损伤期间,复杂的蛋白质结构组装在DNA上。我们的目标是解决这些DNA蛋白复合物的结构,并研究这些结构中发生的动态变化。对于此目的,使用与不同的绿色荧光蛋白(GFP)突变体融合的NER蛋白部分将Ner络合物部分重构到DNA - 基质上。在这里,我们描述了Ner-GFP融合蛋白的重组生产。 GFP荧光的表征与GFP单分子成像的结果一起示出。呈列Ner-GFP融合蛋白的首先结果也是如此。

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