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GCAP-II: isolation and characterization of the circulating form of human uroguanylin.
- 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.
- Subjects :
- Amino Acid Sequence
Calcium-Binding Proteins blood
Calcium-Binding Proteins chemistry
Calcium-Binding Proteins physiology
Cyclic GMP metabolism
Guanylate Cyclase-Activating Proteins
Humans
Molecular Sequence Data
Natriuretic Peptides
Peptides chemistry
Sequence Homology, Amino Acid
Tumor Cells, Cultured
Calcium-Binding Proteins isolation & purification
Subjects
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