Trezeguet V, Labouesse B
Anal Biochem. 1986 May 1;154(2):618-23. doi: 10.1016/0003-2697(86)90037-0.
Quantitative determination of tryptophan at the picomole level is described, using the ATP-[32P]PPi isotopic exchange reaction catalyzed by tryptophanyl-tRNA synthetase. Sensitivity limits of 500 fmol were obtained. The presence of other amino acids at a 1000-fold excess over tryptophan did not interfere significantly with the quantitative determination of tryptophan. The specificity of the reaction was checked using five tryptophan analogs. These analogs did not prevent the determination of tryptophan when present in the same concentration range as tryptophan. When sensitive determination of a single amino acid is needed, the ATP-[32P]PPi exchange reaction catalyzed by aminoacyl-tRNA synthetases is suggested as a general method and as an alternative to HPLC procedures.
本文描述了使用色氨酰 - tRNA合成酶催化的ATP - [32P]PPi同位素交换反应,对皮摩尔水平的色氨酸进行定量测定。获得了500飞摩尔的灵敏度极限。其他氨基酸的存在量比色氨酸高1000倍时,对色氨酸的定量测定没有显著干扰。使用五种色氨酸类似物检查了反应的特异性。当这些类似物与色氨酸处于相同浓度范围时,它们不会妨碍色氨酸的测定。当需要灵敏测定单一氨基酸时,建议将氨酰 - tRNA合成酶催化的ATP - [32P]PPi交换反应作为一种通用方法,作为高效液相色谱法的替代方法。