Conventional 2D-PAGE is cumbersome, slow and difficult to automate. Although, multidimensional, high performance capillary chromatography, electrophoresis and electrochromatography are robust and fully automatable, they are bottlenecked by their inherently serial column operation. These shortcomings can be circumvented by adopting a 2D platform which utilizes several new electrofocusing methods that are based on a novel gradient-monolith technology. The use of monolithic chromatography packings allows us to design a platform which has many of the advantages of chromatographic operation, e.g., automation, in a highly parallelized platform while the use of novel in situ fixed gradients will permit implementation of a new set of equilibrium gradient methods on this platform, specifically, electrofocusing based on conductivity gradients, size-exclusion gradients and pH gradients. The ability to do this in a microchip format is enabled by the recent emergence of technologies for photoinitiated polymerization and gradient functionalization of monolithic packings combined with the development of alternative electrofocusing methods for protein separation. Some key implications of 2D electrofocusing are (1) that the final location and width of protein peaks are independent of their initial distribution, (2) that multiple sample pulses may be loaded onto the platform to increase the amount of low-abundance proteins, and (3) that portions of the sample load can be temporarily sequestered (upstream) or eluted (downstream) off-chip to reduce the high-abundance protein burden during processing. This application seeks to demonstrate two or more of these novel 1D electrofocusing techniques in gradient monolithic packings and then combine them into a 2D microchip. Public Health Relevance Statement: The ability to build a 2D electrofocusing platform in a microchip format is enabled by the recent emergence of photoinitiated polymerization and gradient functionalization of monolithic packings combined with the development of alternative electrofocusing methods for protein separation. This project seeks to demonstrate two or more of these novel 1D electrofocusing techniques in gradient monolithic packings and then combine them into a 2D microchip. It will also develop many of the engineering fundamentals needed for multidimensional platform simulations, microscale process integration and chip design.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21RR023146-02
Application #
7939904
Study Section
Special Emphasis Panel (ZRR1-BT-B (01))
Program Officer
Friedman, Fred K
Project Start
2009-09-24
Project End
2011-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$300,616
Indirect Cost
Name
Washington State University
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
041485301
City
Pullman
State
WA
Country
United States
Zip Code
99164
Liu, Bingwen; Cong, Yongzheng; Ivory, Cornelius F (2014) Counterflow isotachophoresis in a monolithic column. J Sep Sci 37:2395-402
Liu, Bingwen; Ivory, Cornelius F (2013) Isotachophoresis with counterflow in an open capillary: computer simulation and experimental validation. J Sep Sci 36:1986-95