@inproceedings{49f50fd4b98a46428863876a00ef5e27,
title = "Single-molecule fluorescence microscopy on nucleotide excision repair complexes using GFP fusion proteins",
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 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",
keywords = "METIS-130078, IR-96419",
author = "Segers-Nolten, {Gezina M.J.} and Suzanne Rademakers and Wim Vermeulen and Lenferink, {Aufrid T.M.} and Cornelis Otto and Jan Hoeijmakers and Jan Greve",
year = "2000",
month = jan,
day = "11",
doi = "10.1117/12.410629",
language = "Undefined",
isbn = "0-8194-3820-0",
series = "SPIE proceedings",
publisher = "SPIE",
pages = "97--105",
editor = "Karsten Koenig and Tanke, {Hans J.} and Herbert Schneckenburger",
booktitle = "Laser Microscopy",
address = "United States",
note = "Laser microscopy ; Conference date: 01-12-2000 Through 01-12-2000",
}