Publications
2019
de Wijn R, Hennig O, Roche J, Engilberge S, Rollet K, Fernandez-Millan P, Brillet K, Betat H, Mörl M, Roussel A, Girard E, Mueller-Dieckmann C, Fox G C, Olieric V, Gavira J A, Lorber B, Sauter C
A simple and versatile microfluidic device for efficient biomacromolecule crystallization and structural analysis by serial crystallography Journal Article
In: IUCrJ, vol. 6, no. Pt 3, pp. 454-464, 2019, ISBN: 31098026.
Abstract | Links | BibTeX | Tags: ChipX3 counter-diffusion crystallization ligand soaking macromolecule microfluidics protein structure room temperature seeding serial crystallography trace fluorescent labeling, ENNIFAR, FRUGIER, Unité ARN
@article{,
title = {A simple and versatile microfluidic device for efficient biomacromolecule crystallization and structural analysis by serial crystallography},
author = {R de Wijn and O Hennig and J Roche and S Engilberge and K Rollet and P Fernandez-Millan and K Brillet and H Betat and M Mörl and A Roussel and E Girard and C Mueller-Dieckmann and G C Fox and V Olieric and J A Gavira and B Lorber and C Sauter},
url = {https://www.ncbi.nlm.nih.gov/pubmed/31098026?dopt=Abstract},
doi = {10.1107/S2052252519003622},
isbn = {31098026},
year = {2019},
date = {2019-01-01},
journal = {IUCrJ},
volume = {6},
number = {Pt 3},
pages = {454-464},
abstract = {Determining optimal conditions for the production of well diffracting crystals is a key step in every biocrystallography project. Here, a microfluidic device is described that enables the production of crystals by counter-diffusion and their direct on-chip analysis by serial crystallography at room temperature. Nine 'non-model' and diverse biomacromolecules, including seven soluble proteins, a membrane protein and an RNA duplex, were crystallized and treated on-chip with a variety of standard techniques including micro-seeding, crystal soaking with ligands and crystal detection by fluorescence. Furthermore, the crystal structures of four proteins and an RNA were determined based on serial data collected on four synchrotron beamlines, demonstrating the general applicability of this multipurpose chip concept.},
keywords = {ChipX3 counter-diffusion crystallization ligand soaking macromolecule microfluidics protein structure room temperature seeding serial crystallography trace fluorescent labeling, ENNIFAR, FRUGIER, Unité ARN},
pubstate = {published},
tppubtype = {article}
}
Determining optimal conditions for the production of well diffracting crystals is a key step in every biocrystallography project. Here, a microfluidic device is described that enables the production of crystals by counter-diffusion and their direct on-chip analysis by serial crystallography at room temperature. Nine 'non-model' and diverse biomacromolecules, including seven soluble proteins, a membrane protein and an RNA duplex, were crystallized and treated on-chip with a variety of standard techniques including micro-seeding, crystal soaking with ligands and crystal detection by fluorescence. Furthermore, the crystal structures of four proteins and an RNA were determined based on serial data collected on four synchrotron beamlines, demonstrating the general applicability of this multipurpose chip concept.