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Published January 13, 2010 | Supplemental Material + Accepted Version
Journal Article Open

User-Loaded SlipChip for Equipment-Free Multiplexed Nanoliter-Scale Experiments

Abstract

This paper describes a microfluidic approach to perform multiplexed nanoliter-scale experiments by combining a sample with multiple different reagents, each at multiple mixing ratios. This approach employs a user-loaded, equipment-free SlipChip. The mixing ratios, characterized by diluting a fluorescent dye, could be controlled by the volume of each of the combined wells. The SlipChip design was validated on an ∼12 nL scale by screening the conditions for crystallization of glutaryl-CoA dehydrogenase from Burkholderia pseudomallei against 48 different reagents; each reagent was tested at 11 different mixing ratios, for a total of 528 crystallization trials. The total consumption of the protein sample was ∼10 µL. Conditions for crystallization were successfully identified. The crystallization experiments were successfully scaled up in well plates using the conditions identified in the SlipChip. Crystals were characterized by X-ray diffraction and provided a protein structure in a different space group and at a higher resolution than the structure obtained by conventional methods. In this work, this user-loaded SlipChip has been shown to reliably handle fluids of diverse physicochemical properties, such as viscosities and surface tensions. Quantitative measurements of fluorescent intensities and high-resolution imaging were straighforward to perform in these glass SlipChips. Surface chemistry was controlled using fluorinated lubricating fluid, analogous to the fluorinated carrier fluid used in plug-based crystallization. Thus, we expect this approach to be valuable in a number of areas beyond protein crystallization, especially those areas where droplet-based microfluidic systems have demonstrated successes, including measurements of enzyme kinetics and blood coagulation, cell-based assays, and chemical reactions.

Additional Information

© 2009 American Chemical Society. Published In Issue: January 13, 2010. Article ASAP: December 14, 2009. Received: October 07, 2009. This work was supported in part by NIH Roadmap for Medical Research R01 GM075827, by the NIH Protein Structure Initiative Specialized Centers Grant U54 GM074961 (ATCG3D), and by the NIH Director's Pioneer Award (1DP1OD003584). Use of the Argonne National Laboratory GM/CA beamlines at the Advanced Photon Source was supported by the U.S. Department of Energy, Basic Energy Sciences, Office of Science, under Contract No. DE-AC02-06CH11357. GM/CA CAT has been funded in whole or in part with Federal funds from the National Cancer Institute (Y1-CO-1020) and the National Institute of General Medical Science (Y1-GM-1104). We thank Kevin Nichols for providing the movie S1, frames of which were used to create Figure 1; James Norris of the University of Chicago for the generous gift of RC; and SSGCID for the samples of glutaryl-CoA dehydrogenase. SSGCID is supported by Federal Contract No. HHSN272200700057C from NIAID to the Seattle Biomedical Research Institute and its collaborating subcontractors. We thank Elizabeth B. Haney and Heidi Park for contributions to writing and editing this manuscript. We thank Bart Staker for checking the structure of glutaryl-CoA dehydrogenase for PDB deposition. Supporting Information Chemicals and materials, detailed experimental procedures, additional figures and tables, and two supporting movies. This material is available free of charge via the Internet at http://pubs.acs.org.

Attached Files

Accepted Version - nihms-159791.pdf

Supplemental Material - Ismagilov_JACS_2010_user_loaded_SlipChip_132_106_111_LL_WD_supp_info.pdf

Supplemental Material - ja908555n_si_002.mpg

Supplemental Material - ja908555n_si_003.avi

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Additional details

Created:
August 19, 2023
Modified:
October 24, 2023