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Lab-on-a-chip Device To Speed Proteomics Research

Date:
May 3, 2007
Source:
DOE/Lawrence Berkeley National Laboratory
Summary:
Future proteomics research should see a substantial acceleration with the development of a new device that provides the first monolithic interface between mass spectrometry and silicon/silica-based microfluidic "lab-on-a-chip" technologies. This new device is called a multinozzle nanoelectrospray emitter array.

This zoom-in Scanning Electron Microscope image shows a five-nozzle M3 emitter, where each nozzle measures 10x12 microns.
Credit: Department of Energy’s Lawrence Berkeley National Laboratory

In recent years, the science of biology has been dominated by genomics – the study of genes and their functions. The genomics era is now making way for the era of proteomics – the study of the proteins that genes encode.

Future proteomics research should see a substantial acceleration with the development of a new device that provides the first monolithic interface between mass spectrometry and silicon/silica-based microfluidic “lab-on-a-chip” technologies. This new device, called a multinozzle nanoelectrospray emitter array, was developed by scientists with the U.S. Department of Energy’s Lawrence Berkeley National Laboratory (Berkeley Lab).

“Proteomics has become an indispensable tool in biological research, be it diagnostics, therapeutics, bioenergy or stem cell research, and mass spectrometry is proteomics’ enabling technology,” said Daojing Wang, a scientist with Berkeley Lab’s Life Sciences Division who leads the proteomics research group and was the principal investigator behind the development of the multinozzle nanoelectrospray emitter.

“Lab-on-a-chip technology has enormous potential for proteomics research,” Wang said, “but for this potential to be fully realized, a major advance in interfacing microfluidics with mass spectrometry is needed. Our device provides that interface.”

When the Human Genome Project was completed in 2003, giving scientists a complete catalogue of human DNA, the next big effort focused on genomics, identifying DNA sequences that code for proteins, aka, genes. With the identification of each and every new gene, the emphasis shifts to determining the biochemical function of its associated proteins.

All biological cells are constructed from aggregations of proteins that interact with other protein aggregations like an elaborate, finely choreographed network of interdependent machines. This biomolecular machinery also controls nearly every chemical process inside a cell, and forms much of the connectivity that enable cells to come together into tissues and organs. One of the first steps in proteomics research is to determine the identity and modifications of individual proteins that make up a cell or tissue sample. The principal means of doing this is through mass spectrometry.

Mass spectrometers use a combination of ionization and magnets to separate a protein’s constituent peptides. Detection and analysis of this mass spectrum can then be used to identify the protein and quantify its presence in a sample. The most popular technique today for ionizing a protein’s constituents for mass spectrometry is to liquefy the protein and send it through electrically charged capillaries – a technique known as electrospray ionization. One of the best candidates for high throughput integration of the detection and analysis processes is to interface the mass spectrometers with lab-on-a-chip technology, where biological fluids are introduced onto a microprocessor chip. However, microfluidic analysis of proteins has been a separate process from mass spectrometry - until now.

“Ours is the first report of a silicon/silica microfluidic channel that is integrated monolithically with a multinozzle nanoelectrospray emitter,” said Wang. “This paves the way for the large scale integration of mass spectrometry and lab-on-a-chip analysis in proteomics research.”

Each emitter consists of a parallel array of silica nozzles protruding out from a hollow silicon sliver with a conduit size of 100 x 10 microns. Multiple nozzles (100 nozzles per millimeter was a typical density) were used rather than single nozzles in order to reduce the pressure and clogging problems that arise as the microfluidic channels on a chip downsize to a nanometer scale. The emitters and their nozzles were produced from a silicon wafer, with the dimension and number of nozzles systematically and precisely controlled during the fabrication process. Fabrication required the use of only a single mask and involved photolithographic patterning and various etching processes.

Said Peidong Yang, “Once integrated with a mass spectrometer, our microfabricated monolithic multinozzle emitters achieved a sensitivity and stability in peptide and protein detection comparable to commercial silica-based capillary nanoelectrospray tips. This indicates that our emitters could serve as a critical component in a fully integrated silicon/silica-based micro total analysis system for proteomics.”

Added Daojing Wang, “This is also the first report of a multinozzle emitter that can be fabricated through standard microfabrication processes. In addition to having lower back pressure and higher sensitivity, multinozzle emitters also provide a means to systematically study the electrospray ionization processes because the size of each nozzle and density of nozzles on the emitters can be adjusted.”

According to Wang and Yang, the fabrication and application of the microfabricated monolithic multinozzle emitters, called “M3 emitters” for short, could be commercialized immediately and should be highly competitive with current silica capillary emitters in terms of cost and mass production.

“We are now in the process of creating a chip that integrates sample processing and preparation as well as detection and analysis,” said Wang. “The ability to perform the full process on a single chip has enormous commercial potential.”

Wang and Peidong Yang, a leading nanoscience authority with Berkeley Lab’s Molecular Foundry and Materials Sciences Division, and also a chemistry professor with the University of California’s Berkeley campus, co-authored a paper on this work which is being published by the American Chemical Society (ACS). The paper, which is now available in the on-line version. is entitled: “Microfabricated Monolithic Multinozzle Emitters for Nanoelectrospray Mass Spectrometry.”

Other authors of the ACS paper were Woong Kim, a postdoctoral fellow in the Molecular Foundry, and Mingquan Guo, a postdoctoral fellow in the Life Sciences Division.

Berkeley lab has filed for a patent on this technology. The research was supported by a grant from the National Institutes of Health, with some of the work done at Berkeley Lab’s Molecular Foundry, which is supported by the Office of Science in the U.S. Department of Energy.


Story Source:

The above story is based on materials provided by DOE/Lawrence Berkeley National Laboratory. Note: Materials may be edited for content and length.


Cite This Page:

DOE/Lawrence Berkeley National Laboratory. "Lab-on-a-chip Device To Speed Proteomics Research." ScienceDaily. ScienceDaily, 3 May 2007. <www.sciencedaily.com/releases/2007/05/070502143620.htm>.
DOE/Lawrence Berkeley National Laboratory. (2007, May 3). Lab-on-a-chip Device To Speed Proteomics Research. ScienceDaily. Retrieved September 16, 2014 from www.sciencedaily.com/releases/2007/05/070502143620.htm
DOE/Lawrence Berkeley National Laboratory. "Lab-on-a-chip Device To Speed Proteomics Research." ScienceDaily. www.sciencedaily.com/releases/2007/05/070502143620.htm (accessed September 16, 2014).

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