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Met -enkephalin

Leu-enkephalin, Met-enkephalin [59141-40-11 polypeptide multiple tissues endogenous opiates... [Pg.169]

In the anterior pituitary gland (see Hormones, anteriorpituitaryhormones), both adrenocorticotropic hormones (ACTH) and the endogenous opiate hormone, P-endorphin, are synthesized from a common prohormone (2) (see Opioids,endogenous). In the adrenal medulla, five to seven copies of another opiate hormone, methionine—enkephalin (Met-enkephalin), and one copy of leucine—enkephalin (Leu-enkephalin) are synthesized from each precursor molecule (3). [Pg.171]

Biosynthesis. Three separate genes encode the opioid peptides (see Fig. 1). Enkephalin is derived from preproenkephalin A, which contains six copies of Met-enkephalin and extended peptides, and one copy of Leu-enkephalin (62—66). ( -Endorphin is one of the many products of POMC, and represents the N-terminal 31 amino acids of P-Hpotropin (67,68). Three different dynorphin peptides are derived from the third opioid gene, preproenkephalin B, or preprodynorphin (69). The dynorphin peptides include dynorphin A, dynorphin B, and a-neo-endorphin. [Pg.203]

At the time of the discovery of Met-enkephalin, its sequence was observed to be identical to that of residues 61—65 contained in the C-fragment of the pituitary hormone p-Hpotropin [12584-99-5] (p-LPH) (see Hormones), first isolated in 1964 (11). In 1976, the isolation of a larger peptide fragment, P-endorphin [60617-12-1] that also displayed opiate-like activity was reported (12). This peptide s 31-amino-acid sequence comprised residues 61—91 of P-LPH. Subsequentiy, another potent opioid peptide, dynorphin [72957-38-17, was isolated from pituitary (13). The first five amino acids (qv) of this 17-amino-acid peptide are identical to the Leu-enkephalin sequence (see Table 1). [Pg.444]

Group II consists of the enkephalins which come from the 267-aniino acid piecuisoi pro-enkephalin A [88402-54-4] (Fig. 2). This proteia contains four copies of Met-enkephalin, one copy of Leu-enkephalin, and the extended peptides Met-enkephalin-Arg -Phe (the last Met-enkephalin sequence ia Fig. 2) and Met-enkephalin-Arg -Gly -Leu (the fourth Met-enkephalin sequence ia Fig. 2) (25,26). AH of these products ate formed by trypsin-like cleavage between pairs of basic residues. The extended enkephalin peptides are further cleaved by carboxypeptidase E (27) to form authentic Met-enkephalin. [Pg.446]

The opioid peptides vary in their binding affinities for the multiple opioid receptor types. Leu- and Met-enkephalin have a higher affinity for 5-receptors than for the other opioid receptor types (68), whereas the dynorphin peptides have a higher affinity for K-sites (69). P-Endorphin binds with equal affinity to both p- and 5-receptors, but binds with lower affinity to K-sites (70). The existence of a P-endorphin-selective receptor, the S-receptor, has been postulated whether this site is actually a separate P-endorphin-selective receptor or is a subtype of a classical opioid receptor is a matter of controversy (71,72). The existence of opioid receptor subtypes in general is quite controversial although there is some evidence for subtypes of p- (73), 5-(74), and K-receptors (72,75), confirmation of which may be obtained by future molecular cloning studies. [Pg.447]

Several enzymes, none of which are completely specific for the enkephalins, are known to cleave Leu- and Met-enkephalin at various peptide bonds. The main enzymes that degrade enkephalin are 2inc metaHopeptidases. The first enkephalin-degrading enzyme to be identified, an aminopeptidase which cleaves the amino terminal Tyr-Gly bond (179), has been shown to be aminopeptidase-N (APN) (180). It is a cytoplasmic enzyme which is uniformly distributed throughout the brain. The increased analgesic activity of synthetic enkephalins substituted by D-amino acids at position 2, eg,... [Pg.451]

Figure 4. Enzymatic hydrolysis of met-enkephalin (2.5 nmol) showing the sequential release of amino acids and the final mixture. The amino acids were identified from the retention times of the standard amino acid mixture 9, Gly 12, Tyr 14, Met 17, Phe. (Reprinted from reference 5. Copyright 1987 American Chemical Society.)... Figure 4. Enzymatic hydrolysis of met-enkephalin (2.5 nmol) showing the sequential release of amino acids and the final mixture. The amino acids were identified from the retention times of the standard amino acid mixture 9, Gly 12, Tyr 14, Met 17, Phe. (Reprinted from reference 5. Copyright 1987 American Chemical Society.)...
Some propeptides produce multiple copies of similar peptides (met-enkephalin and leu-enkephalin act on the same delta opioid receptor). [Pg.253]

Guyenet, P. G. Aghajanian, G. K. (1979). ACh, substance P and met-enkephalin in the locus coeruleus pharmacological evidence for independent sites of action. [Pg.102]

Thyroliberin (thyrotropin-releasing hormone, Endomorphin 1 Methionine (MET)-enkephalin Cholecystokinin-8S (CCK-8S)... [Pg.19]


See other pages where Met -enkephalin is mentioned: [Pg.533]    [Pg.611]    [Pg.172]    [Pg.201]    [Pg.202]    [Pg.203]    [Pg.544]    [Pg.544]    [Pg.444]    [Pg.445]    [Pg.445]    [Pg.445]    [Pg.450]    [Pg.450]    [Pg.450]    [Pg.259]    [Pg.380]    [Pg.381]    [Pg.381]    [Pg.381]    [Pg.76]    [Pg.486]    [Pg.904]    [Pg.906]    [Pg.864]    [Pg.63]    [Pg.133]    [Pg.329]    [Pg.378]    [Pg.382]    [Pg.7]    [Pg.864]    [Pg.403]    [Pg.100]    [Pg.170]    [Pg.244]    [Pg.137]    [Pg.316]   
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