Identification of regions within the third FnIII-like domain of the IL-5R alpha involved in IL-5 interaction


Autoria(s): Czabotar, PE; Holland, J; Sanderson, CJ
Data(s)

01/01/2000

Resumo

Previously, two binding sites for interleukin 5 (IL-5) were identified on the IL-5 receptor alpha chain (IL-5R alpha). They are located within the CD loop of the first fibronectin type III (FnIII)-like domain and the EF loop of the second FnIII-like domain. The first binding site was identified by exploiting the different abilities of human IL-5R alpha (hIL-5R alpha) and mouse IL-5R alpha (mIL-5R alpha) to bind hIL-5. Here we show that ovine IL-5 (oIL-5) has the ability to activate the hIL-5R alpha but not the mIL-5R alpha. By using chimeras of the mIL-5R alpha and hIL-5R alpha we demonstrate that residues within the first and third FnIII-like domains of mIL-5R alpha are responsible for this lack of activity. Furthermore, mutation of residues on hIL-5R alpha to mIL-5R alpha within the predicted DE and FG loop regions of the third FnIII domain reduces oIL-5 activity, These results show that regions of the third FnIII domain of IL-5R alpha are involved in binding, in addition to the regions in domains one and two of the IL-5R alpha that were identified in an earlier study. (C) 2000 Academic Press.

Identificador

http://espace.library.uq.edu.au/view/UQ:36537

Idioma(s)

eng

Palavras-Chave #Biochemistry & Molecular Biology #Cell Biology #Immunology #Cytokine Receptor #Interleukin 5 #Il-5 #Il5-r Alpha #Recombinant Human Interleukin-5 #Stimulating Factor-receptor #Alpha-chain #Crystal-structure #Growth-hormone #Cell-growth #Swiss-model #Gm-csf #Binding #Ligand
Tipo

Journal Article