Miyazato M, Nakazato M, Shiomi K, Kangawa K, Matsuo H, Matsukura S
Department of Medicine, Miyazaki Medical College, Japan.
Regul Pept. 1994 Jan 13;49(3):203-10. doi: 10.1016/0167-0115(94)90142-2.
Using a highly sensitive and specific radioimmunoassay (RIA) for the N-terminal hexadecapeptide of islet amyloid polypeptide (IAPP), we isolated two N-terminal fragments of IAPP from rat pancreas. They were identified as IAPP(1-16) and IAPP(1-17) by amino acid sequencing. The two fragments were also found in rat plasma. IAPP(1-37) was the major molecular form of rat IAPP, IAPP(1-16) and IAPP(1-17) accounting for 6.0% and 32.3% of the immunoreactivity for the N-terminal region of the peptide in pancreata of normally fed rats. In human pancreas, the N-terminal fragments of IAPP were not present, indicating that the processing of IAPP in the pancreas differs between human and rat. Food deprivation increased the molar ratios of IAPP(1-16) and IAPP(1-17) to IAPP(1-37) in comparison to values for fed rats. Identification of novel fragments of IAPP, in addition to IAPP(1-37), offers a promise for the elucidation of the physiological function of IAPP and the identification of factors that regulate the biosynthesis and catabolism of the peptide.
我们使用一种针对胰岛淀粉样多肽(IAPP)N端十六肽的高灵敏度和特异性放射免疫分析(RIA)方法,从大鼠胰腺中分离出了IAPP的两个N端片段。通过氨基酸测序,它们被鉴定为IAPP(1 - 16)和IAPP(1 - 17)。这两个片段在大鼠血浆中也被发现。IAPP(1 - 37)是大鼠IAPP的主要分子形式,在正常喂食大鼠的胰腺中,IAPP(1 - 16)和IAPP(1 - 17)分别占该肽N端区域免疫反应性的6.0%和32.3%。在人类胰腺中,不存在IAPP的N端片段,这表明人类和大鼠胰腺中IAPP的加工过程存在差异。与喂食大鼠相比,禁食增加了IAPP(1 - 16)和IAPP(1 - 17)与IAPP(1 - 37)的摩尔比。除了IAPP(1 - 37)之外,IAPP新片段的鉴定为阐明IAPP的生理功能以及鉴定调节该肽生物合成和分解代谢的因素提供了希望。