Cohen S A, Michaud D P
Millipore Corp., Milford, Massachusetts 01757.
Anal Biochem. 1993 Jun;211(2):279-87. doi: 10.1006/abio.1993.1270.
A highly reactive amine derivatizing reagent, 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate, has been synthesized. In a rapid, one-step procedure, the compound reacts with amino acids to form stable unsymmetric urea derivatives which are readily amenable to analysis by reversed phase HPLC. Studies on derivatization conditions demonstrate excellent derivative yield over the pH range 8.2-10.0. Maximal yields are observed with a molar reagent excess of approximately three or greater. The reaction is extremely tolerant of common buffer salts and detergents, with no discernible decrease in reaction yield with well-buffered samples. Selective fluorescence detection of the derivatives with excitation at 250 nm and emission at 395 nm allows for the direct injection of the reaction mixture with no significant interference from the only major fluorescent reagent by-product, 6-aminoquinoline. Separation of the derivatized amino acids has been optimized on a C18 column with complete resolution in less than 35 min. Excellent response linearity is demonstrated over the concentration range 2.5-200 microM for all hydrolysate amino acids. Detection limits range from 40 fmol for phenylalanine to 800 fmol for cystine. Good compositional data could be obtained from the analysis of derivatized protein hydrolysates containing as little as 30 ng of sample.
已合成一种高反应性胺衍生化试剂6-氨基喹啉基-N-羟基琥珀酰亚胺基氨基甲酸酯。在快速的一步法中,该化合物与氨基酸反应形成稳定的不对称脲衍生物,这些衍生物易于通过反相高效液相色谱进行分析。衍生化条件研究表明,在pH值8.2 - 10.0范围内,衍生物产率优异。当试剂摩尔过量约为三倍或更高时,可观察到最大产率。该反应对常见缓冲盐和去污剂具有极强的耐受性,对于缓冲良好的样品,反应产率无明显下降。在250 nm激发波长和395 nm发射波长下对衍生物进行选择性荧光检测,可直接进样反应混合物,唯一主要的荧光试剂副产物6-氨基喹啉无明显干扰。在C18柱上对衍生化氨基酸的分离进行了优化,不到35分钟即可实现完全分离。对于所有水解氨基酸,在2.5 - 200 microM浓度范围内均表现出优异的响应线性。检测限范围从苯丙氨酸的40 fmol到胱氨酸的800 fmol。从对仅含30 ng样品的衍生化蛋白质水解产物的分析中可获得良好的组成数据。