| Literature DB >> 27241728 |
Shuo Sui1, Yuxi Wang1, Kristopher W Kolewe1, Vukica Srajer2, Robert Henning2, Jessica D Schiffman1, Christos Dimitrakopoulos1, Sarah L Perry1.
Abstract
Microfluidic strategies to enable the growth and subsequent serial crystallographic analysis of micro-crystals have the potential to facilitate both structural characterization and dynamic structural studies of protein targets that have been resistant to single-crystal strategies. However, adapting microfluidic crystallization platforms for micro-crystallography requires a dramatic decrease in the overall device thickness. We report a robust strategy for the straightforward incorporation of single-layer graphene into ultra-thin microfluidic devices. This architecture allows for a total material thickness of only ∼1 μm, facilitating on-chip X-ray diffraction analysis while creating a sample environment that is stable against significant water loss over several weeks. We demonstrate excellent signal-to-noise in our X-ray diffraction measurements using a 1.5 μs polychromatic X-ray exposure, and validate our approach via on-chip structure determination using hen egg white lysozyme (HEWL) as a model system. Although this work is focused on the use of graphene for protein crystallography, we anticipate that this technology should find utility in a wide range of both X-ray and other lab on a chip applications.Entities:
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Year: 2016 PMID: 27241728 PMCID: PMC4970872 DOI: 10.1039/c6lc00451b
Source DB: PubMed Journal: Lab Chip ISSN: 1473-0189 Impact factor: 6.799