Identification of two related pentapeptides from the brain with potent opiate agonist activity

Nature, 258(5536), 577-580

DOI 10.1038/258577a0 PMID 1207728

Abstract

Enkephalin, a natural ligand for opiate receptors is composed of the pentapepides H-Tyr-Gly-Gly-Phe-Met-OH and H-Tyr-Gly-Gly-Phe-Leu-OH. The evidence is based on the determination of the amino acid sequence of natural enkephalin by the dansyl-Edman procedure and by mass spectrometry followed by synthesis and comparison of the natural and synthetic peptides.

Topics

enkephalin discovery opiate receptor natural ligand, Hughes Kosterlitz endogenous opioid pentapeptide identification, met-enkephalin leu-enkephalin amino acid sequence brain, endogenous opioid peptide opiate agonist activity, natural opiate ligand brain pentapeptide characterization, enkephalin mass spectrometry dansyl Edman sequencing, endogenous opioid system discovery neuroscience, opioid receptor ligand identification 1975 landmark, neuropeptide enkephalin synthesis comparison natural synthetic
PMID 1207728 1207728 DOI 10.1038/258577a0 10.1038/258577a0

Cite this article

Hughes, J., Smith, T. W., Kosterlitz, H. W., Fothergill, L. A., Morgan, B. A., & Morris, H. R. (1975). Identification of two related pentapeptides from the brain with potent opiate agonist activity. *Nature*, *258*(5536), 577-580. https://doi.org/10.1038/258577a0

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