Separation of phenylthiohydantoin amino acids by capillary electrochromatography
✍ Scribed by Thomas Mueller; Ulrike C. Posch; Herbert H. Lindner
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 176 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0173-0835
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✦ Synopsis
Abstract
Capillary electrochromatography (CEC) was employed as a rapid and high‐efficiency method for the isocratic separation of all 20 important phenylthiohydantoin (PTH) amino acids, the end products of Edman degradation during N‐terminal protein sequencing. For this purpose, 75 μm ID fused‐silica capillaries were packed with standard 3 μm Hypersil octadecyl silica (ODS) particles using a two‐step column fabrication process, which represents a fast, reliable and efficient means of producing long‐term stable columns. The influence of solvent composition, pH, type of buffer cation, buffer concentration, and temperature on retention behavior of PTH amino acids was investigated. Same‐day and day‐to‐day reproducibility of the retention times (over a period of two months) were found to be better than 3%. When comparing this new technique with traditional reversed phase‐high performance liquid chromatography (RP‐HPLC) methods applied in automated protein sequenators, CEC shows essentially shorter separation times and superior resolution.
📜 SIMILAR VOLUMES
All common phenyhhiohydantoin amino acids derived from sequencing are identifiable in 6 to 9 min with an isocratic method based on buffered aqueous acetonitrile, an ODS stationary phase, and programmed flow which increases during the run. With constant flow the analysis requires 16 min. The effects
A high-performance liquid chromatographic analytical system is described for the separation, identification, and quantitation of phenylthiohydantoin (PTH) derivatives of all amino acids normally encountered in proteins. The system employs reverse-phase chromatography on a PBondapak phenylalkyl stati