Roper Stephen M, Weindel Annette L, Dietzen Dennis J
Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, USA.
Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
Methods Mol Biol. 2022;2546:55-64. doi: 10.1007/978-1-0716-2565-1_6.
Analysis of clinically relevant amino acids using ion exchange chromatography coupled to photometric/fluorescent detection has been an indispensable component in the detection of inborn errors of metabolism for six decades. Detection of amino acids using mass spectrometry offers advantages in speed and analytic specificity. Employing methanol extraction and controlled butylation, C8 reversed-phase chromatography, and MS/MS detection, 32 amino acids are quantified in 20 min with clinically appropriate imprecision in plasma, urine, and cerebrospinal fluid (CSF). Quantitation is linear to 2500 μM, and limits of detection are at least 1.0 μM. Important isobaric amino acids are distinguished by chromatography or by unique patterns of fragmentation following collision-induced dissociation (CID). The technique employs commercially available reagents and may be expanded and customized for specific clinical or research settings.
六十年来,使用离子交换色谱结合光度/荧光检测对临床相关氨基酸进行分析一直是先天性代谢缺陷检测中不可或缺的组成部分。使用质谱法检测氨基酸在速度和分析特异性方面具有优势。采用甲醇萃取和可控丁基化、C8反相色谱以及串联质谱检测,可在20分钟内对血浆、尿液和脑脊液中的32种氨基酸进行定量,且不精密度在临床可接受范围内。定量线性范围达2500 μM,检测限至少为1.0 μM。重要的等压氨基酸可通过色谱法或碰撞诱导解离(CID)后的独特碎片模式加以区分。该技术使用市售试剂,可针对特定临床或研究环境进行扩展和定制。