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Growing Protein Crystals with Distinct Dimensions Using Automated Crystallization Coupled with In Situ Dynamic Light Scattering.
Baitan, Daniela; Schubert, Robin; Meyer, Arne; Dierks, Karsten; Perbandt, Markus; Betzel, Christian.
Afiliación
  • Baitan D; Xtal Concepts GmbH; Institute for Biochemistry and Molecular Biology, Laboratory for Structural Biology of Infection and Inflammation c/o DESY, University of Hamburg.
  • Schubert R; Institute for Biochemistry and Molecular Biology, Laboratory for Structural Biology of Infection and Inflammation c/o DESY, University of Hamburg; The Hamburg Center for Ultrafast Imaging, University of Hamburg.
  • Meyer A; Xtal Concepts GmbH.
  • Dierks K; Xtal Concepts GmbH.
  • Perbandt M; Institute for Biochemistry and Molecular Biology, Laboratory for Structural Biology of Infection and Inflammation c/o DESY, University of Hamburg; The Hamburg Center for Ultrafast Imaging, University of Hamburg.
  • Betzel C; Institute for Biochemistry and Molecular Biology, Laboratory for Structural Biology of Infection and Inflammation c/o DESY, University of Hamburg; The Hamburg Center for Ultrafast Imaging, University of Hamburg; christian.betzel@uni-hamburg.de.
J Vis Exp ; (138)2018 08 14.
Article en En | MEDLINE | ID: mdl-30175998
ABSTRACT
The automated crystallization device is a patented technique1 especially developed for monitoring protein crystallization experiments with the aim to precisely maneuver the nucleation and crystal growth towards desired sizes of protein crystals. The controlled crystallization is based on sample investigation with in situ Dynamic Light Scattering (DLS) while all visual changes in the droplet are monitored online with the help of a microscope coupled to a CCD camera, thus enabling a full investigation of the protein droplet during all stages of crystallization. The use of in situ DLS measurements throughout the entire experiment allows a precise identification of the highly supersaturated protein solution transitioning to a new phase - the formation of crystal nuclei. By identifying the protein nucleation stage, the crystallization can be optimized from large protein crystals to the production of protein microcrystals. The experimental protocol shows an interactive crystallization approach based on precise automated steps such as precipitant addition, water evaporation for inducing high supersaturation, and sample dilution for slowing induced homogeneous nucleation or reversing phase transitions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas / Cristalización / Dispersión Dinámica de Luz Idioma: En Revista: J Vis Exp Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas / Cristalización / Dispersión Dinámica de Luz Idioma: En Revista: J Vis Exp Año: 2018 Tipo del documento: Article
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