Codini M, Palmerini C A, Fini C, Lucarelli C, Floridi A
Dipartimento di Medicina Sperimentale e Scienze Biochimiche, Università di Perugia, Italy.
J Chromatogr. 1991 Jan 4;536(1-2):337-41. doi: 10.1016/s0021-9673(01)89267-0.
A rapid and accurate method is described for the determination of prolyl peptides in urine, with specific reference to the dipeptide prolylhydroxyproline, and free hydroxyproline and proline. Free amino acids and peptides were isolated from urine on cation-exchange minicolumns, and free imino acids and prolyl-N-terminal peptides were selectively derivatized with 4-chloro-7-nitrobenzofurazan, after reaction of amino acids and N-terminal aminoacyl peptides with o-phthalaldehyde. The highly fluorescent adducts of imino acids and prolyl peptides were separated on a Spherisorb ODS 2 column by isocratic elution for 12 min using as mobile phase 17.5 mM aqueous trifluoracetic acid solution containing 12.5% acetonitrile (eluent A), followed by gradient elution from eluent A to 40% of 17.5 mM aqueous trifluoroacetic acid solution containing 80% acetonitrile in 20 min. Analytes of interest, in particular the dipeptide prolylhydroxyproline, can be easily quantified by fluorimetric detection (epsilon ex = 470 nm, epsilon em = 530 nm) without interference from primary amino-containing compounds.
本文描述了一种快速、准确测定尿液中脯氨酰肽的方法,特别针对二肽脯氨酰羟脯氨酸、游离羟脯氨酸和脯氨酸。游离氨基酸和肽在阳离子交换微型柱上从尿液中分离出来,在氨基酸和N端氨基酰肽与邻苯二甲醛反应后,游离亚氨基酸和脯氨酰N端肽用4-氯-7-硝基苯并呋喃选择性衍生化。亚氨基酸和脯氨酰肽的高荧光加合物在Spherisorb ODS 2柱上通过等度洗脱12分钟进行分离,流动相为含12.5%乙腈的17.5 mM三氟乙酸水溶液(洗脱液A),随后在20分钟内从洗脱液A梯度洗脱至含80%乙腈的17.5 mM三氟乙酸水溶液的40%。感兴趣的分析物,特别是二肽脯氨酰羟脯氨酸,可通过荧光检测(激发波长εex = 470 nm,发射波长εem = 530 nm)轻松定量,不受含伯氨基化合物的干扰。