Chaves Das Neves H J, Vasconcelos A M
J Chromatogr. 1987 Apr 17;392:249-58. doi: 10.1016/s0021-9673(01)94270-0.
Amino acids and the amino acid amides glutamine and asparagine can be simultaneously derivatized to the corresponding N,O(S)-tert.-butyldimethylsilyl derivatives in a one-step reaction with N-methyl-N-(tert.-butyldimethylsilyl)trifluoroacetamide in acetonitrile. The solution is used directly for gas chromatography (GC). Losses due to evaporation steps are avoided. Except for the more basic amino acids, derivatization occurs at room temperature. Lysine, arginine and histidine require additional heating at 150 degrees C for 2.5 h in order to complete derivatization. The derivatization has high reproducibility. The response factors relative to norvaline or cycloleucine lie between 0.40 and 1.30. Arginine is the most difficult amino acid to derivatize. The size of the tert.-butyldimethylsilyl (TBDMS) group prevents multiple silylation of the nitrogen atoms. Only a single peak is observed for each compound. Twenty-seven amino acid (and glutamine and asparagine) derivatives were simultaneously chromatographed and well separated in a single run on a 25 m X 0.20 mm I.D. glass capillary column coated with OV-1. The TBDMS derivatives possess very characteristic EI mass spectra at 70 eV, with intense diagnostic ions. This makes them very appropriate for GC-mass spectrometric (MS) work and selected ion monitoring GC-MS at the picomole level. The detection limit for arginine as the TBDMS derivative is less than 0.3 ng. The usefulness of the method is illustrated by the detection of amino acids in a peptide hydrolysate obtained from 1 microgram of bovin insulin B-chain.
氨基酸以及氨基酸酰胺谷氨酰胺和天冬酰胺,可在乙腈中与N - 甲基 - N -(叔丁基二甲基甲硅烷基)三氟乙酰胺通过一步反应同时衍生化为相应的N,O(S)-叔丁基二甲基甲硅烷基衍生物。该溶液可直接用于气相色谱(GC)分析,避免了因蒸发步骤导致的损失。除碱性较强的氨基酸外,衍生化反应在室温下进行。赖氨酸、精氨酸和组氨酸需要在150℃额外加热2.5小时以完成衍生化。该衍生化反应具有高重现性。相对于正缬氨酸或环亮氨酸的响应因子在0.40至1.30之间。精氨酸是最难衍生化的氨基酸。叔丁基二甲基甲硅烷基(TBDMS)基团的大小可防止氮原子的多次硅烷化。每种化合物仅观察到一个峰。27种氨基酸(以及谷氨酰胺和天冬酰胺)衍生物在一根25 m×0.20 mm内径、涂覆有OV - 1的玻璃毛细管柱上一次进样即可同时进行色谱分离且分离效果良好。TBDMS衍生物在70 eV下具有非常特征性的电子轰击(EI)质谱,带有强诊断离子。这使得它们非常适合用于气相色谱 - 质谱联用(GC - MS)分析以及皮摩尔级别的选择离子监测GC - MS分析。精氨酸的TBDMS衍生物的检测限小于0.3 ng。从1微克牛胰岛素B链获得的肽水解产物中氨基酸的检测证明了该方法的实用性。