| Autor: |
Pepin, Marie-Claude, Beauchemin, Michel, Collins, Catherine, Plamondon, Josée, O'Connor-Mccourt, Maureen D. |
| Zdroj: |
FEBS Letters; January 1995, Vol. 377 Issue: 3 p368-372, 5p |
| Abstrakt: |
There are two TGF- βbinding subdomains in the extracellular domain of receptor type III (proximal and distal in relation to the transmembrane domain). Here we present an extension of our analysis of the proximal binding site of receptor type III. Due to the original deletion mutagenesis strategy, our proximal binding site contained 19 amino acids from the N-terminal part of the receptor. By deleting these, we demonstrated that they did not contribute to the binding ability of the proximal binding site. We also produced a soluble, secreted form of the proximal binding site and demonstrated that it was able to bind TGF- β. Finally, we analyzed the role of the three asparagine residues (580, 591, 595) that are located in the region of the receptor that is necessary for expression of a functional proximal binding site, and found that mutation of these residues individually to alanine did not affect ligand binding. |
| Databáze: |
Supplemental Index |
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