From screen to structure with a harvestable microfluidic device

Vivian Stojanoff, Jean Jakoncic, Deena A. Oren, V. Nagarajan, Jens Christian Navarro Poulsen, Melanie A. Adams-Cioaba, Terese Bergfors, Morten O.A. Sommer

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


Advances in automation have facilitated the widespread adoption of high-throughput vapour-diffusion methods for initial crystallization screening. However, for many proteins, screening thousands of crystallization conditions fails to yield crystals of sufficient quality for structural characterization. Here, the rates of crystal identification for thaumatin, catalase and myoglobin using microfluidic Crystal Former devices and sitting-drop vapour-diffusion plates are compared. It is shown that the Crystal Former results in a greater number of identified initial crystallization conditions compared with vapour diffusion. Furthermore, crystals of thaumatin and lysozyme obtained in the Crystal Former were used directly for structure determination both in situ and upon harvesting and cryocooling. On the basis of these results, a crystallization strategy is proposed that uses multiple methods with distinct kinetic trajectories through the protein phase diagram to increase the output of crystallization pipelines.

Original languageEnglish
Pages (from-to)971-975
Number of pages5
JournalActa Crystallographica Section F: Structural Biology and Crystallization Communications
Issue number8
StatePublished - Aug 2011
Externally publishedYes


  • Crystal Former
  • liquid-liquid diffusion
  • microfluidics
  • protein crystallization
  • structural biology


Dive into the research topics of 'From screen to structure with a harvestable microfluidic device'. Together they form a unique fingerprint.

Cite this