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
Separation of amino acid phenylthiohydantoins by high-performance liquid chromatography on phenylalkyl support
โ Scribed by Louis E. Henderson; Terry D. Copeland; Stephen Oroszlan
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 527 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
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 stationary phase. PTH derivatives of all amino acids can be identified and quantitated in a single 30-min analysis using linear gradient elution. The method can be applied equally well to the separation of methyl esters of the PTH-derivatized decarboxylic amino acids. The sensitivity of the method extends into the range of less than IO pmol.
๐ SIMILAR VOLUMES
A comparison of the separation of the common phenylthiohydantoin derivatives of amino acids on DuPont octadecylsilane with that obtained with Ultrasphere octadecylsilane supports is given together with the effect of acetate, phosphate, and trifluoroacetate buffers in the elution solvents. An importa