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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1994-10-6
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pubmed:abstractText |
The properties of di- and tri-peptides containing 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) in second position suggest that the message domain of opioid peptides can be composed of only two residues [Temussi, P. A., Salvadori, S., Amodeo, P., Guerrini, R., Tomatis, R., Lazarus, L. H., Picone, D. & Tancredi, T. (1994) Biochem. Biophys. Res. Commun. 198, 933-939]. As a crucial test of the possibility that the Tyr-Tic segment be a message domain in longer peptide sequences, we have inserted it in the sequences of two typical opioid peptides: [Leu]enkephalin, a non-selective agonist, and dermorphin, a selective mu agonist. Here we report the synthesis and biological activity of [L-Tic2]enkephalin, [L-Tic2]dermorphin, [L-Tic2]dermorphin carboxylic acid and [D-Tic2]dermorphin: all [L-Tic2]peptides were converted from agonists to delta-selective antagonists. The NMR conformational study in a dimethylsulfoxide/water cryoprotective mixture at low temperature shows diagnostic side-chain--side-chain NOEs in the spectra of all [L-Tic2]peptides and hints that the 90 degrees arrangement of the the two aromatic rings found in the cis-Tyr-L-Tic moiety, typical of N-methyl naltrindole and other delta-selective opiate antagonists, is responsible for the antagonist activity of all these peptides.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,2,3,4-tetrahydroisoquinoline...,
http://linkedlifedata.com/resource/pubmed/chemical/Enkephalins,
http://linkedlifedata.com/resource/pubmed/chemical/Isoquinolines,
http://linkedlifedata.com/resource/pubmed/chemical/Narcotic Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Opioid Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrahydroisoquinolines,
http://linkedlifedata.com/resource/pubmed/chemical/dermorphin
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0014-2956
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
224
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
241-7
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pubmed:dateRevised |
2007-7-23
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pubmed:meshHeading |
pubmed-meshheading:8076645-Amino Acid Sequence,
pubmed-meshheading:8076645-Animals,
pubmed-meshheading:8076645-Brain,
pubmed-meshheading:8076645-Enkephalins,
pubmed-meshheading:8076645-Guinea Pigs,
pubmed-meshheading:8076645-Isoquinolines,
pubmed-meshheading:8076645-Magnetic Resonance Spectroscopy,
pubmed-meshheading:8076645-Mice,
pubmed-meshheading:8076645-Models, Molecular,
pubmed-meshheading:8076645-Molecular Sequence Data,
pubmed-meshheading:8076645-Narcotic Antagonists,
pubmed-meshheading:8076645-Oligopeptides,
pubmed-meshheading:8076645-Opioid Peptides,
pubmed-meshheading:8076645-Protein Conformation,
pubmed-meshheading:8076645-Radioligand Assay,
pubmed-meshheading:8076645-Rats,
pubmed-meshheading:8076645-Tetrahydroisoquinolines
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pubmed:year |
1994
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pubmed:articleTitle |
Conversion of enkephalin and dermorphin into delta-selective opioid antagonists by single-residue substitution.
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pubmed:affiliation |
ICMIB del CNR, Napoli, Italy.
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pubmed:publicationType |
Journal Article,
In Vitro
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