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

  • Ine Segers-Nolten
  • , Suzanne Rademakers
  • , Wim Vermeulen
  • , Aufried Lenferink
  • , Cees Otto
  • , Jan Hoeijmakers
  • , Jan Greve

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)97-105
Number of pages9
JournalProceedings of SPIE - The International Society for Optical Engineering
Volume4164
DOIs
Publication statusPublished - 2000
Externally publishedYes

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