The goal of this research is to develop the techniques of microcolumn liquid chromatography and apply them to problems in ultramicro analysis of biological systems. Microcolumn LC has the capability to handle nanoliter to picoliter sample volumes and offers femtomole to sub-attomole detection limits. Research is focused on three topics: 1. Microscale analysis: Research will be aimed at development of techniques for chemical analysis of single cells. Studies will include techniques for sample manipulation and microscale chemistry at the nanoliter scale. Development of an Edman degradation protein sequencing scheme at the femtomole level will be a highlight of this work. Another project will concern the simultaneous analysis of the size and chemical contents of single neurosecretory vesicles. 2. Detection technology: Sensitive detectors based on electrochemistry and fluorescence have been developed. The current need is for additional detection schemes which are sensitive but less selective. Microelectrospray techniques, which permit introduction of non-volatile analytes directly into gas or vacuum phase, have been developed. These techniques work at the sub-nanoliter per second flow rates characteristic of microcolumn LC. Microelectrospray coupled with mass spectrometry and photoionization detection will be studied. The goal will be to provide high quality information, such as can be obtained from mass spectra, at the attomole level. 3. Two-dimensional LC: For highly complex samples, two dimensional systems (LC/LC) offer greater resolving power than traditional one dimensional chromatography. Two-dimensional systems using microcolumn LC in both dimensions will be developed. With these systems, the high resolving power of two-dimensional separations can be applied to difficult problems involving detecting trace components in complex interfering matrices, such as the measurement of neuropeptides in single cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039515-05
Application #
3296568
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1988-08-01
Project End
1994-11-30
Budget Start
1992-12-01
Budget End
1993-11-30
Support Year
5
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Arts and Sciences
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Patel, Kamlesh D; Jerkovich, Anton D; Link, Jason C et al. (2004) In-depth characterization of slurry packed capillary columns with 1.0-microm nonporous particles using reversed-phase isocratic ultrahigh-pressure liquid chromatography. Anal Chem 76:5777-86
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MacNair, J E; Patel, K D; Jorgenson, J W (1999) Ultrahigh-pressure reversed-phase capillary liquid chromatography: isocratic and gradient elution using columns packed with 1.0-micron particles. Anal Chem 71:700-8
Lan, K; Jorgenson, J W (1999) Automated measurement of peak widths for the determination of peak capacity in complex chromatograms. Anal Chem 71:709-14
Opiteck, G J; Ramirez, S M; Jorgenson, J W et al. (1998) Comprehensive two-dimensional high-performance liquid chromatography for the isolation of overexpressed proteins and proteome mapping. Anal Biochem 258:349-61
Lan, K; Jorgenson, J W (1998) Pressure-induced retention variations in reversed-phase alternate-pumping recycle chromatography. Anal Chem 70:2773-82
Hsieh, S; Dreisewerd, K; van der Schors, R C et al. (1998) Separation and identification of peptides in single neurons by microcolumn liquid chromatography-matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and postsource decay analysis. Anal Chem 70:1847-52
MacNair, J E; Opiteck, G J; Jorgenson, J W et al. (1997) Rapid separation and characterization of protein and peptide mixtures using 1.5 microns diameter non-porous silica in packed capillary liquid chromatography/mass spectrometry. Rapid Commun Mass Spectrom 11:1279-85

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