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GCAP-II: isolation and characterization of the circulating form of human uroguanylin.

Authors :
Hess R
Kuhn M
Schulz-Knappe P
Raida M
Fuchs M
Klodt J
Adermann K
Kaever V
Cetin Y
Forssmann WG
Source :
FEBS letters [FEBS Lett] 1995 Oct 23; Vol. 374 (1), pp. 34-8.
Publication Year :
1995

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.

Details

Language :
English
ISSN :
0014-5793
Volume :
374
Issue :
1
Database :
MEDLINE
Journal :
FEBS letters
Publication Type :
Academic Journal
Accession number :
7589507
Full Text :
https://doi.org/10.1016/0014-5793(95)01075-p