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@ARTICLE{Sadoine:849675,
      author       = {Sadoine, Mayuri and Cerminara, Michele and Fitter, Jörg
                      and Katranidis, Alexandros},
      title        = {{P}reparation of {C}ell-free {S}ynthesized {P}roteins
                      {S}electively {D}ouble {L}abeled for {S}ingle-molecule
                      {FRET} {S}tudies},
      journal      = {Bio-protocol},
      volume       = {8},
      number       = {12},
      issn         = {2331-8325},
      address      = {Sunnyvale, CA},
      publisher    = {bio-protocol.org},
      reportid     = {FZJ-2018-03811},
      pages        = {1},
      year         = {2018},
      abstract     = {Single-molecule FRET (smFRET) is a powerful tool to
                      investigate molecular structures and conformational changes
                      of biological molecules. The technique requires protein
                      samples that are site-specifically equipped with a pair of
                      donor and acceptor fluorophores. Here, we present a detailed
                      protocol for preparing double-labeled proteins for smFRET
                      studies. The protocol describes two cell-free approaches to
                      achieve a selective label scheme that allows the highest
                      possible accuracy in inter‐dye distance determination.},
      cin          = {ICS-5},
      ddc          = {570},
      cid          = {I:(DE-Juel1)ICS-5-20110106},
      pnm          = {551 - Functional Macromolecules and Complexes (POF3-551)},
      pid          = {G:(DE-HGF)POF3-551},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000457962400003},
      doi          = {10.21769/BioProtoc.2881},
      url          = {https://juser.fz-juelich.de/record/849675},
}