Skip to content
Licensed Unlicensed Requires Authentication Published by De Gruyter March 5, 2007

Human dipeptidyl peptidase III acts as a post-proline-cleaving enzyme on endomorphins

  • Marina Baršun , Nina Jajčanin , Bojana Vukelić , Jasminka Špoljarić and Marija Abramić
From the journal Biological Chemistry

Abstract

Dipeptidyl peptidase III (DPP III) is a zinc exopeptidase with an implied role in the mammalian pain-modulatory system owing to its high affinity for enkephalins and localisation in the superficial laminae of the spinal cord dorsal horn. Our study revealed that this human enzyme hydrolyses opioid peptides belonging to three new groups, endomorphins, hemorphins and exorphins. The enzymatic hydrolysis products of endomorphin-1 were separated and quantified by capillary electrophoresis and the kinetic parameters were determined for human DPP III and rat DPP IV. Both peptidases cleave endomorphin-1 at comparable rates, with liberation of the N-terminal Tyr-Pro. This is the first evidence of DPP III acting as an endomorphin-cleaving enzyme.

:

Corresponding author

References

Abramić, M., Zubanović, M., and Vitale, Lj. (1988). Dipeptidyl peptidase III from human erythrocytes. Biol. Chem. Hoppe-Seyler369, 29–38.10.1515/bchm3.1988.369.1.29Search in Google Scholar

Abramić, M., Schleuder, D., Dolovčak, Lj., Schröder, W., Strupat, K., Šagi, D., Peter-Katalinić, J., and Vitale, L. (2000). Human and rat dipeptidyl peptidase III: biochemical and mass spectrometric arguments for similarities and differences. Biol. Chem.381, 1233–1243.10.1515/BC.2000.151Search in Google Scholar

Abramić, M., Šimaga, Š., Osmak, M., Čičin-Šain, L., Vukelić, B., Vlahoviček, K., and Dolovčak, L. (2004). Highly reactive cysteine residues are part of the substrate binding site of mammalian dipeptidyl peptidases III. Int. J. Biochem. Cell Biol.36, 434–446.10.1016/S1357-2725(03)00267-XSearch in Google Scholar

Chiba, T., Li, Y.-H., Yamane, T., Ogikubo, O., Fukuoka, M., Arai, R., Takahashi, S., Ohtsuka, T., Ohkubo, I., and Matsui, N. (2003). Inhibition of recombinant dipeptidyl peptidase III by synthetic hemorphin-like peptides. Peptides24, 773–778.10.1016/S0196-9781(03)00119-0Search in Google Scholar

Chu, T.G. and Orlowski, M. (1985). Soluble metalloendopeptidase from rat brain: action on enkephalin-containing peptides and other bioactive peptides. Endocrinology116, 1418–1425.10.1210/endo-116-4-1418Search in Google Scholar

Cunningham, D.F. and O'Connor, B. (1997). Proline specific peptidases. Biochim. Biophys. Acta1343, 160–186.10.1016/S0167-4838(97)00134-9Search in Google Scholar

de la Baume, S., Yi, C.C., Schwartz, J.C., Chaillet, P., Marcais-Collado, H., and Constantin, J. (1983). Participation of both “enkephalinase” and aminopeptidase activities in the metabolism of endogenous enkephalins. Neuroscience8, 143–151.10.1016/0306-4522(83)90033-7Search in Google Scholar

Ellis, S. and Nuenke, J.M. (1967). Dipeptidyl arylamidase III of pituitary: purification and characterization. J. Biol. Chem.242, 4623–4629.10.1016/S0021-9258(18)99503-7Search in Google Scholar

Fukasawa, K., Fukasawa, K.M., Kanai, M., Fujii, S., Hirose, J., and Harada, M. (1998). Dipeptidyl peptidase III is a zinc metallo-exopeptidase: molecular cloning and expression. Biochem. J.329, 275–282.10.1042/bj3290275Search in Google Scholar PubMed PubMed Central

Fukasawa, K., Fukasawa, K.M, Iwamoto, H., Hirose, J., and Harada, M. (1999). The HELLGH motif of rat liver dipeptidyl peptidase III is involved in zinc coordination and the catalytic activity of the enzyme. Biochemistry38, 8299–8303.10.1021/bi9904959Search in Google Scholar PubMed

Gorenstein, C. and Snyder, S.H. (1979). Two distinct enkephalinases: solubilization, partial purification and separation from angiotensin converting enzyme. Life Sci.25, 2065–2070.10.1016/0024-3205(79)90198-XSearch in Google Scholar

Guieu, R., Fenouillet, E., Devaux, C., Fajloun, Z., Carrega, L., Sabatier, J. M., Sauze, N., and Marguet, D. (2006). CD26 modulates nociception in mice via its dipeptidyl-peptidase IV activity. Behav. Brain Res.166, 230–235.10.1016/j.bbr.2005.08.003Search in Google Scholar

Huang, J., Kim, J., Ramamurthy, P., and Jones, T.H.D. (1992). The purification, specificity, and role of dipeptidyl peptidase III in Dictyostelium discoideum. Exp. Mycol.16, 102–109.10.1016/0147-5975(92)90016-KSearch in Google Scholar

Ikehara, Y., Ogata, S., and Misumi, Y. (1994). Dipeptidyl-peptidase IV from rat liver. In: Methods in Enzymology, Vol. 244, A.J. Barrett, ed. (San Diego, USA: Academic Press), pp. 215–227.10.1016/0076-6879(94)44018-2Search in Google Scholar

Lee, C.-M. and Snyder, S.H (1982). Dipeptidyl-aminopeptidase III of rat brain: Selective affinity for enkephalin and angiotensin. J. Biol. Chem.257, 12043–12050.10.1016/S0021-9258(18)33674-3Search in Google Scholar

Lee, H.-J. and Wilson, I.B. (1971). Enzymatic parameters: measurement of V and Km. Biochim. Biophys. Acta242, 519–522.10.1016/0005-2744(71)90144-6Search in Google Scholar

Martin-Schild, S., Gerall, A.A., Kastin, A.J., and Zadina, J.E. (1999). Differential distribution of endomorphin 1- and endomorphin 2-like immunoreactivities in the CNS of the rodent. J. Comp. Neurol.405, 450–471.10.1002/(SICI)1096-9861(19990322)405:4<450::AID-CNE2>3.0.CO;2-#Search in Google Scholar

Mazzocco, C., Fukasawa, K.M., Auguste, P., and Puiroux, J. (2003). Characterization of a functionally expressed dipeptidyl aminopeptidase III from Drosophila melanogaster. Eur. J. Biochem.270, 3074–3082.10.1046/j.1432-1033.2003.03689.xSearch in Google Scholar

McDonald, J.K. (1998). Dipeptidyl-peptidase III. In: Handbook of Proteolytic Enzymes, A.J. Barrett, N.D. Rawlings and J.F. Woessner, eds. (San Diego, USA: Academic Press), pp. 536–538.Search in Google Scholar

McDonald, J.K. and Barrett, A.J. (1986). Mammalian Proteases: A Glossary and Bibliography, Vol. 2: Exopeptidases (London, UK: Academic Press).Search in Google Scholar

Mentlein, R. (1999). Dipeptidyl-peptidase IV (CD26) – role in the inactivation of regulatory peptides. Regul. Peptides85, 9–24.10.1016/S0167-0115(99)00089-0Search in Google Scholar

Nishimura, K. and Hazato, T. (1993). Isolation and identification of an endogenous inhibitor of enkephalin-degrading enzymes from bovine spinal cord. Biochem. Biophys. Res. Commun.194, 713–719.10.1006/bbrc.1993.1880Search in Google Scholar

O'Cuinn, G. (1994). Dipeptidyl aminopeptidase activities of guinea-pig brain. Int. J. Biochem.26, 913–921.Search in Google Scholar

Ohkubo, I., Li, Y.-H., Maeda, T., Yamamoto, Y., Yamane, T., Du, P.-G., and Nishi, K. (1999). Dipeptidyl peptidase III from rat liver cytosol: purification, molecular cloning and immunohistochemical localization. Biol. Chem.380, 1421–1430.10.1515/BC.1999.182Search in Google Scholar

Rasmussen, H.B., Branner, S., Wiberg, F.C., and Wagtmann, N. (2003). Crystal structure of human dipeptidyl peptidase IV/ CD26 in complex with a substrate analog. Nat. Struct. Biol.10, 19–25.10.1038/nsb882Search in Google Scholar

Sakurada, C., Sakurada, S., Hayashi, T., Katsuyama, S., Tan-No, K., and Sakurada, T. (2003). Degradation of endomorphin-2 at the supraspinal level in mice is initiated by dipeptidyl peptidase IV: an in vitro and in vivo study. Biochem. Pharmacol.66, 653–661.10.1016/S0006-2952(03)00391-5Search in Google Scholar

Sato, H., Kimura, K., Yamamoto, Y., and Hazato, T. (2003). Activity of DPP III in human cerebrospinal fluid derived from patients with pain. Jpn. J. Anesthesiol.52, 257–263.Search in Google Scholar

Shrimpton, C.N., Smith, A.I., and Lew, R.A. (2002). Soluble metalloendopeptidases and neuroendocrine signaling. Endocr. Rev.23, 647–664.10.1210/er.2001-0032Search in Google Scholar

Smyth, M. and O'Cuinn, G. (1994). Dipeptidyl aminopeptidase III of guinea-pig brain: specificity for short oligopeptide sequences. J. Neurochem.63, 1439–1445.10.1046/j.1471-4159.1994.63041439.xSearch in Google Scholar

Strausberg, R.L., Feingold, E.A., Grouse, L.H., Derge, J.G., Klausner R.D., Collins, F.S., Wagner, L., Shenmen, C.M., Schuler, G.D., Altschul, S.F., et al. (2002). Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Natl. Acad. Sci. USA99, 16899–16903.Search in Google Scholar

Thoma, R., Löffler, B., Stihle, M., Huber, W., Ruf, A., and Hennig., M. (2003). Structural basis of proline-specific exopeptidase activity as observed in human dipeptidyl peptidase-IV. Structure11, 947–959.10.1016/S0969-2126(03)00160-6Search in Google Scholar

Thompson, J.D., Higgins, D.G., and Gibson, T.J. (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res.22, 4673–4680.10.1093/nar/22.22.4673Search in Google Scholar

Tömböly, C., Péter, A., and Tóth, G. (2002). In vitro quantitative study of the degradation of endomorphins. Peptides23, 1573–1580.10.1016/S0196-9781(02)00100-6Search in Google Scholar

Unsworth, C.D., Hughes, J., and Morley, J.S. (1982). O-Sulphated Leu-enkephalin in brain. Nature295, 519–522.10.1038/295519a0Search in Google Scholar

van Amsterdam, J.G.C., van Buuren, K.J.H., and Soudijn, W. (1983). Purification and characterization of enkephalin-degrading enzymes from calf-brain striatum. Biochem. Biophys. Res. Commun.115, 632–641.10.1016/S0006-291X(83)80191-0Search in Google Scholar

Watanabe, Y., Kumagai, Y., and Fujimoto, Y. (1990). Presence of a dipeptidyl aminopeptidase III in Saccharomyces cerevisiae. Chem. Pharm. Bull.38, 246–248.10.1248/cpb.38.246Search in Google Scholar

Yamamoto, M., Chikuma, T., Yajima, R., Hirano, H., Yamamoto, Y., Nishi, K., Ohkubo, I., and Kato, T. (2002). Axonal transport of puromycin-sensitive aminopeptidase in rat sciatic nerves. Neurosci. Res.42, 133–140.10.1016/S0168-0102(01)00319-4Search in Google Scholar

Yamamoto, M., Chikuma, T., Yamashita, A., Yamaguchi, M., Hojo, H., Ozeki, Y., Ahmed, M., and Kato, T. (2003). Anterograde axonal transport of endopeptidase 24.15 in rat sciatic nerves. Neurochem. Int.42, 231–237.Search in Google Scholar

Published Online: 2007-03-05
Published in Print: 2007-03-01

©2007 by Walter de Gruyter Berlin New York

Downloaded on 23.4.2024 from https://www.degruyter.com/document/doi/10.1515/BC.2007.039/html
Scroll to top button