TY - JOUR
T1 - Fabrication of X-ray compatible microfluidic platforms for protein crystallization
AU - Guha, Sudipto
AU - Perry, Sarah L.
AU - Pawate, Ashtamurthy S.
AU - Kenis, Paul J.A.
N1 - Funding Information:
This work was funded by NIH ( R01 GM086727 ) and a NIH Kirschstein Predoctoral Fellowship from the National Institute of Biomedical Imaging and Bioengineering ( F31 EB008330 ). Use of the Advanced Photon Source was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences , under Contract No. DE-AC02-06CH11357. Use of the LS-CAT Sector 21 was supported by the Michigan Economic Development Corporation and the Michigan Technology Tri-Corridor for the support of this research program (Grant 085P1000817 ).
PY - 2012/11
Y1 - 2012/11
N2 - This paper reports a method for fabricating multilayer microfluidic protein crystallization platforms using different materials to achieve X-ray transparency and compatibility with crystallization reagents. To validate this approach, three soluble proteins, lysozyme, thaumatin, and ribonuclease A were crystallized on-chip, followed by on-chip diffraction data collection. We also report a chip with an array of wells for screening different conditions that consume a minimal amount of protein solution as compared to traditional screening methods. A large number of high quality isomorphous protein crystals can be grown in the wells, after which slices of X-ray data can be collected from many crystals still residing within the wells. Complete protein structures can be obtained by merging these slices of data followed by further processing with crystallography software. This approach of using an X-ray transparent chip for screening, crystal growth, and X-ray data collection enables room temperature data collection from many crystals mounted in parallel, which thus eliminates crystal handling and minimizes radiation damage to the crystals.
AB - This paper reports a method for fabricating multilayer microfluidic protein crystallization platforms using different materials to achieve X-ray transparency and compatibility with crystallization reagents. To validate this approach, three soluble proteins, lysozyme, thaumatin, and ribonuclease A were crystallized on-chip, followed by on-chip diffraction data collection. We also report a chip with an array of wells for screening different conditions that consume a minimal amount of protein solution as compared to traditional screening methods. A large number of high quality isomorphous protein crystals can be grown in the wells, after which slices of X-ray data can be collected from many crystals still residing within the wells. Complete protein structures can be obtained by merging these slices of data followed by further processing with crystallography software. This approach of using an X-ray transparent chip for screening, crystal growth, and X-ray data collection enables room temperature data collection from many crystals mounted in parallel, which thus eliminates crystal handling and minimizes radiation damage to the crystals.
KW - Crystallography
KW - Microfabrication
KW - Protein crystallization
KW - Structure determination
KW - X-ray transparency
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U2 - 10.1016/j.snb.2012.08.048
DO - 10.1016/j.snb.2012.08.048
M3 - Article
AN - SCOPUS:84868108495
SN - 0925-4005
VL - 174
SP - 1
EP - 9
JO - Sensors and Actuators, B: Chemical
JF - Sensors and Actuators, B: Chemical
ER -