| Autor: |
Wada, T., Nagata, Y., Nagahisa, H., Okutomi, K., Ha, S.H., Ohnuki, T., Kanaya, T., Matsumura, M., Todokoro, K. |
| Zdroj: |
Biochemical and Biophysical Research Communications; August 24, 1995, Vol. 213 Issue: 3 p1091-1098, 8p |
| Abstrakt: |
Thrombopoietin (Tpo) is a specific cytokine which regulates megakaryocyte differentiation and maturation. We isolated a truncated mouse Tpo cDNA, the product of which turned out to function neither as an active Tpo variant nor as an antagonist. To define the functional domains of the Tpo molecule further, various truncated and point-mutated Tpo molecules were prepared and their biological activity was assayed. It was found that deletion of the amino terminal side of a potential proteolytic cleavage site, Arg-Arg motif, caused complete loss of Tpo's activity, and that point-mutants lacking one of four conserved cysteine residues lost Tpo activity. We also noticed that Tpo activity was inhibited by the reducing agent. Thus, it was concluded that the amino terminal half of the Tpo is sufficient for Tpo activity, and that the cysteine residues, especially the last cysteine residue located two amino acids away from the Arg-Arg motif, are critical for this activity.Copyright 1995, 1999 Academic Press, Inc. |
| Databáze: |
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