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Journal Article

Ethoxylate Polymer-Based 96-Well Screen for Protein Crystallization

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Demmer,  Ulrike       
Department of Molecular Membrane Biology, Max Planck Institute of Biophysics, Max Planck Society;

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Ermler,  Ulrich       
Department of Molecular Membrane Biology, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Demmer, U., Lemaire, O., Belhamri, M., & Ermler, U. (2023). Ethoxylate Polymer-Based 96-Well Screen for Protein Crystallization. Crystals, 13: 1519. doi:10.3390/cryst13101519.


Cite as: https://hdl.handle.net/21.11116/0000-000D-D457-2
Abstract
Crystallization is the limiting step in X-ray structure determination of biological macromolecules. As crystallization experiments can be largely automatized, the diversity of precipitant solutions is often the determinant factor to obtain crystals of high quality. Here, we introduce a 96-well screening kit of crystallization conditions, centered on three ethoxylate-based organic polymers as precipitants and various additional compounds to promote crystal formation. This crystallization screen was tested on various non-standard proteins from bacteria and archaea. Structure determination succeeded for seven out of thirteen targets based on crystals that frequently diffracted to a higher resolution than those obtained with commercially available screening kits. Crystallization hits were rarely similar among the three ethoxylate-based organic polymers and, in comparison, with already available crystallization screens. Hence, the presented crystallization screen is an efficient tool to complement other screens and increase the likelihood of growing crystals suitable for X-ray structure determination.