Hyphenation of capillary high-performance liquid chromatography with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for nano-scale screening of single-bead combinatorial libraries
| Autor: | Dietrich A. Volmer, Oliver Keil, Holger Deppe, Tammy LeRiche |
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| Rok vydání: | 2002 |
| Předmět: |
MALDI imaging
Detection limit Chromatography Protein mass spectrometry Chemistry Ion-mobility spectrometry Organic Chemistry Analytical chemistry Mass spectrometry Capillary electrophoresis–mass spectrometry Analytical Chemistry Liquid chromatography–mass spectrometry Direct electron ionization liquid chromatography–mass spectrometry interface Spectroscopy |
| Zdroj: | Rapid communications in mass spectrometry : RCM. 16(8) |
| ISSN: | 0951-4198 |
| Popis: | This paper focuses on the technical aspects of chemical screening from 384-well plate nano-scale single-bead combinatorial libraries. The analytical technique utilized is a combination of capillary liquid chromatography with ultraviolet detection and matrix-assisted laser desorption/ionization (MALDI) mass spectrometry. The HPLC/MALDI-MS hyphenation is achieved by means of a micro-fraction collector with a peak detection system that automatically collects the peaks onto the MALDI targets for subsequent characterization. Several experimental parameters such as type of 384-well plate, well-plate sealing foils, and a column-switching procedure were investigated using a small test library of nine components. Additionally, the influence of different MALDI matrices, different MALDI targets and sample-spotting techniques on the MALDI detection sensitivity as well as the ruggedness and sample throughput capacity of this technique were studied. Optimum results for the analytes investigated were obtained with 2,5-dihydroxybenzoic acid using on-line mixing of HPLC effluent and matrix solution. To demonstrate the potential of this capillary HPLC/MALDI-TOFMS method, its application to several single-bead libraries was investigated. The instrumental method allowed for the rapid identification and purity assessment of combinatorial libraries with detection limits down to the higher femtomole level using both UV detection and MALDI mass spectrometry. Copyright © 2002 John Wiley & Sons, Ltd. |
| Databáze: | OpenAIRE |
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