Abstract
Enkephalin, a natural ligand for opiate receptors is composed of the pentapeptides 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.
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References
Terenius, L., Wahlström, A., Acta pharmac. tox., 35, Suppl. 1, 55 (1974).
Terenius, L., and Wahlström, A., Acta physiol. scand., 94, 74–81 (1975).
Hughes, J., Brain Res., 88, 295–308 (1975).
Hughes, J., Smith, T., Morgan, B., and Fothergill, L., Life Sci., 16, 1753–1758 (1975).
Pasternak, G. W., Goodman, R., and Snyder, S. H., Life Sci., 16, 1765–1769 (1975).
Cox, B. M., Opheim, K. E., Teschemacher, H., and Goldstein, A., Life Sci., 16, 1777–1782 (1975).
Penke, B., Ferenczi, R., and Kovacs, K., Analyt. Biochem., 60, 45–50 (1974).
Hartley, B. S., Biochem. J., 119, 805–822 (1970).
Morris, H. R., FEBS Lett., 22, 257–260 (1972).
Morris, H. R., William, D. H., Midwinter, G. G., and Hartley, B. S., Biochem. J., 141, 701–713 (1974).
Hunt, E., Morris, H. R., Biochem. J., 135, 833–843 (1973).
Hughes, J., Kosterlitz, H. W., and Leslie, F. M., Br. J. Pharmac., 53, 371–381 (1975).
Kosterlitz, H. W., and Watt, A. J., Br. J. Pharmac. Chemother., 33, 266–276 (1968).
Li, C. H., Barnafi, L., Chrétien, M., and Chung, D., Nature, 208, 1093–1094 (1965).
Gráf, L., Barát, E., Cseh, G., and Sajgó, M., Biochem. biophys. Acta, 229, 276–278 (1971).
Cseh, G., Bar´t, E., Patthy, A., and Gr´f, L., FEBS Lett., 21, 344–346 (1972).
Teschemacher, H., Opheim, K. E., Cox, B. M., and Goldstein, A., Life Sci., 16, 1771–1776 (1975).
Cox, B. M., Opheim, K. E., Teschemacher, H., and Goldstein, A., Life Sci., 16, 1777–1782 (1975).
Kosterlitz, H. W., Hughes, J., Life Sci., 17, 91–96 (1975).
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Hughes, J., Smith, T., Kosterlitz, H. et al. Identification of two related pentapeptides from the brain with potent opiate agonist activity. Nature 258, 577–579 (1975). https://doi.org/10.1038/258577a0
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DOI: https://doi.org/10.1038/258577a0
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