| Literature DB >> 7589507 |
R Hess1, M Kuhn, P Schulz-Knappe, M Raida, M Fuchs, J Klodt, K Adermann, V Kaever, Y Cetin, W G Forssmann.
Abstract
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.Entities:
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Year: 1995 PMID: 7589507 DOI: 10.1016/0014-5793(95)01075-p
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124