Hess R, Kuhn M, Schulz-Knappe P, Raida M, Fuchs M, Klodt J, Adermann K, Kaever V, Cetin Y, Forssmann W G
Lower Saxony Institute for Peptide Research (IPF), Hannover, Germany.
FEBS Lett. 1995 Oct 23;374(1):34-8. doi: 10.1016/0014-5793(95)01075-p.
The systematic isolation of circulating regulatory peptides which generate cGMP as second messenger resulted in the identification of a novel member of the guanylin family. In the present study we describe the purification and amino acid sequence of a new guanylate cyclase C activating peptide (GCAP-II). GCAP-II contains 24 amino acids in the following sequence: FKTLRTIANDDCELCVNVACTGCL. Its molecular mass is 2597.7 Da. The 16 C-terminal amino acids are identical to uroguanylin from human urine. native and synthetic GCAP-II activate GC-C, the specific guanylate cyclase receptor, of cultured human colon carcinoma (T84) cells. GCAP-II stimulates chloride secretion in isolated human intestinal mucosa mediated by intracellular cGMP increase. GCAP-II specific antibodies were used to localize the peptide by immunohistochemistry in entero-endocrine cells of the colonic mucosa.
对以环鸟苷酸(cGMP)作为第二信使的循环调节肽进行系统分离,从而鉴定出鸟苷酸环化酶激活肽家族的一个新成员。在本研究中,我们描述了一种新的鸟苷酸环化酶C激活肽(GCAP-II)的纯化及氨基酸序列。GCAP-II含有24个氨基酸,序列如下:FKTLRTIANDDCELCVNVACTGCL。其分子量为2597.7道尔顿。C末端的16个氨基酸与人尿中的尿鸟苷酸环化酶激活肽相同。天然和合成的GCAP-II均可激活培养的人结肠癌细胞(T84)中的特异性鸟苷酸环化酶受体GC-C。GCAP-II通过细胞内cGMP增加介导,刺激离体人肠黏膜中的氯离子分泌。使用GCAP-II特异性抗体,通过免疫组织化学法在结肠黏膜的肠内分泌细胞中定位该肽。