Complete primary structure of prostatropin, a prostate epithelial cell growth factor

• Published in: Biochemistry (Easton) 1986-09, Vol.25 (18), p.4988-4993
• Main Authors: Crabb, John W, Armes, L. Gene, Carr, Steven A, Johnson, Charles M, Roberts, Gerald D, Bordoli, Robert S, McKeehan, W. L
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Brain Chemistry; Cattle; Epithelium - drug effects; Fibroblast Growth Factor 2; Fundamental and applied biological sciences. Psychology; Male; Mass Spectrometry; Nerve Tissue Proteins - isolation & purification; Nerve Tissue Proteins - pharmacology; Peptide Fragments - analysis; Prostate - drug effects; Protein hormones. Growth factors. Cytokines; Proteins
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00366a003

Bovine brain prostatropin is a potent and essential mitogen for prostate epithelial cell growth. The major form of prostatropin contains 154 amino acid residues in a single amino terminally blocked chain corresponding to a molecular weight of 17,400. The amino acid sequence of the 150 carboxy-terminal residues of prostatropin was derived by Edman degradation of overlapping peptides primarily generated by cleavage at lysyl and glutamyl residues. Analysis of the amino-terminal tetradecapeptide by fast atom bombardment mass spectrometry identified the blocking group as an acetyl moiety, and tandem mass spectrometry provided the sequence of the first 12 residues. Prostatropin residues 15-154 contain the sequence of bovine brain polypeptides recently described as acidic fibroblast growth factor and class I heparin-binding growth factor. The sequence of the first 25 residues of prostatropin is acetyl-Ala-(Gly, Glu)-Glu-Thr-Thr-Thr-Phe-Thr-Ala-Leu-Thr-Glu-Lys-Phe-Asn-Leu-Pro-Leu-Gly -Asn-Tyr-Lys-Lys-Pro. Reduced and carboxymethylated prostatropin exhibits mitogenic activity, suggesting that disulfide bonds among cysteine residues 30, 61, and 97 are not functionally essential. These results demonstrate by rigorous structural analysis that the brain-derived polypeptide previously described only as a mesenchymal and neuroectodermal cell mitogen is also an epithelial cell growth factor that may be involved in support of prostate hyperplasia and adenocarcinoma.