Lin C C, Chang G G
Department of Biochemistry, National Defense Medical Center, Taipei, Taiwan, Republic of China.
J Protein Chem. 1993 Oct;12(5):627-32. doi: 10.1007/BF01025127.
The active site of pigeon liver malic enzyme was labeled with a fluorescent affinity label, the periodate-oxidized aminopyridine adenine dinucleotide phosphate. The modified enzyme was subjected to proteolytic digestion with trypsin. The resulted peptides were then separated with reversed-phase high-performance liquid chromatography on Waters muBondapak C18 column. Two pure fluorescent peptides were obtained after three runs of the chromatography. The peptides were then subjected to automatic Edman degradation on a Beckman peptide sequencer and subsequently separated and identified with phenylthiohydantoin C18 column. No sequence was obtained. The possible reasons for the failure in sequencing the periodate-oxidized nucleotides labeled active site peptide and some possible pitfalls in using these reagents were discussed.
用荧光亲和标记物——高碘酸盐氧化的氨基吡啶腺嘌呤二核苷酸磷酸对鸽肝苹果酸酶的活性位点进行标记。将修饰后的酶用胰蛋白酶进行蛋白水解消化。然后,所得肽段在沃特世μBondapak C18柱上通过反相高效液相色谱进行分离。经过三轮色谱分离后得到了两个纯的荧光肽段。接着,这些肽段在贝克曼肽测序仪上进行自动埃德曼降解,随后用苯硫代乙内酰脲C18柱进行分离和鉴定。但未获得序列信息。讨论了对高碘酸盐氧化核苷酸标记的活性位点肽段测序失败的可能原因以及使用这些试剂时一些可能存在的问题。