Autor: |
Enghild, J J, Thøgersen, Ida, Oury, T D, Valnickova, Z, Hojrup, P, Crapo, J D |
Jazyk: |
angličtina |
Rok vydání: |
1999 |
Předmět: |
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Zdroj: |
Enghild, J J, Thøgersen, I, Oury, T D, Valnickova, Z, Hojrup, P & Crapo, J D 1999, ' The heparin-binding domain of extracellular superoxide dismutase is proteolytically processed intracellularly during biosynthesis ', Journal of Biological Chemistry, vol. 274, no. 21, pp. 14818-22 . |
Popis: |
Udgivelsesdato: 1999-May-21 Extracellular superoxide dismutase (EC-SOD) is the only known extracellular enzyme designed to scavenge the superoxide anion. The purified enzyme exists in two forms when visualized by reduced SDS-polyacrylamide gel electrophoresis: (i) intact EC-SOD (Trp1-Ala222) containing the C-terminal heparin-binding domain and (ii) cleaved EC-SOD (Trp1-Glu209) without the C-terminal heparin-binding domain. The proteolytic event(s) leading to proteolysis at Glu209-Arg210 and removal of the heparin-binding domain are not known, but may represent an important regulatory mechanism. Removal of the heparin-binding domain affects both the affinity of EC-SOD for and its distribution to the extracellular matrix, in which it is secreted. During the purification of human EC-SOD, the intact/cleaved ratio remains constant, suggesting that proteolytic removal of the heparin-binding domain does not occur during purification (Oury, T. D., Crapo, J. D., Valnickova, Z., and Enghild, J. J. (1996) Biochem. J. 317, 51-57). This was supported by the finding that fresh mouse tissue contains both intact and cleaved EC-SOD. To study other possible mechanisms leading to the formation of cleaved EC-SOD, we examined biosynthesis in cultured rat L2 epithelial-like cells using a pulse-chase protocol. The results of these studies suggest that the heparin-binding domain is removed intracellularly just prior to secretion. In addition, the intact/cleaved EC-SOD ratio appears to be tissue-dependent, implying that the intracellular processing event is regulated in a tissue-specific manner. The existence of this intracellular processing pathway may thus represent a novel regulatory pathway for affecting the distribution and effect of EC-SOD. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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