Choudhury A M, Kenner G W, Moore S, Ramachandran K L, Thorpe W D, Ramage R, Dockray G J, Gregory R A, Hood L, Hunkapiller M
Hoppe Seylers Z Physiol Chem. 1980 Nov;361(11):1719-33. doi: 10.1515/bchm2.1980.361.2.1719.
The previously assigned structure of human big gastrin is revised as a result of sequencing and immunological studies on synthetic peptides. A nonadecapeptide has been synthesized and found to have full immunochemical potency compared with natural human G34 in a radioimmunoassay which is specific for the N-terminal sequence. Syntheses of the peptides were achieved using the stepwise procedure with benzyloxycarbonyl-amino acids and fragment couplings mediated mainly by the dicyclohexylcarbodiimide procedure in the presence of either N-hydroxysuccinimide or 1-hydroxybenzotriazole. Purification of the peptide fragments was by Sephadex LH-20 chromatography and removal of protecting groups was effected using 90% trifluoroacetic acid in the presence of scavengers. Purification of the nonadecapeptide was achieved by high performance liquid chromatography.
由于对合成肽的测序和免疫学研究,人类大胃泌素先前确定的结构被修正。已合成一种十九肽,在针对N端序列的放射免疫分析中,发现其与天然人G34相比具有完全的免疫化学活性。肽的合成采用逐步法,使用苄氧羰基氨基酸,并主要通过二环己基碳二亚胺法在N-羟基琥珀酰亚胺或1-羟基苯并三唑存在下进行片段偶联。肽片段通过Sephadex LH-20色谱法纯化,脱保护基团在清除剂存在下使用90%三氟乙酸进行。十九肽通过高效液相色谱法纯化。