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New page: left|200px<br /> <applet load="1boe" size="450" color="white" frame="true" align="right" spinBox="true" caption="1boe" /> '''STRUCTURE OF THE IGF BINDING DOMAIN OF THE ...
 
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[[Image:1boe.gif|left|200px]]<br />
[[Image:1boe.gif|left|200px]]<br /><applet load="1boe" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1boe" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1boe" />
caption="1boe" />
'''STRUCTURE OF THE IGF BINDING DOMAIN OF THE INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-5 (IGFBP-5): IMPLICATIONS FOR IGF AND IGF-I RECEPTOR INTERACTIONS'''<br />
'''STRUCTURE OF THE IGF BINDING DOMAIN OF THE INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-5 (IGFBP-5): IMPLICATIONS FOR IGF AND IGF-I RECEPTOR INTERACTIONS'''<br />


==Overview==
==Overview==
Binding proteins for insulin-like growth factors (IGFs) IGF-I and IGF-II, known as IGFBPs, control the distribution, function and activity of IGFs, in various cell tissues and body fluids. Insulin-like growth, factor-binding protein-5 (IGFBP-5) is known to modulate the stimulatory, effects of IGFs and is the major IGF-binding protein in bone tissue. We, have expressed two N-terminal fragments of IGFBP-5 in Escherichia coli;, the first encodes the N-terminal domain of the protein (residues 1-104), and the second, mini-IGFBP-5, comprises residues Ala40 to Ile92. We show, that the entire IGFBP-5 protein contains only one high-affinity binding, site for IGFs, located in mini-IGFBP-5. The solution structure of, mini-IGFBP-5, determined by nuclear magnetic resonance spectroscopy, discloses a rigid, globular structure that consists of a centrally located, three-stranded anti-parallel beta-sheet. Its scaffold is stabilized, further by two inside packed disulfide bridges. The binding to IGFs, which, is in the nanomolar range, involves conserved Leu and Val residues, localized in a hydrophobic patch on the surface of the IGFBP-5 protein., Remarkably, the IGF-I receptor binding assays of IGFBP-5 showed that, IGFBP-5 inhibits the binding of IGFs to the IGF-I receptor, resulting in, reduction of receptor stimulation and autophosphorylation. Compared with, the full-length IGFBP-5, the smaller N-terminal fragments were less, efficient inhibitors of the IGF-I receptor binding of IGFs.
Binding proteins for insulin-like growth factors (IGFs) IGF-I and IGF-II, known as IGFBPs, control the distribution, function and activity of IGFs in various cell tissues and body fluids. Insulin-like growth factor-binding protein-5 (IGFBP-5) is known to modulate the stimulatory effects of IGFs and is the major IGF-binding protein in bone tissue. We have expressed two N-terminal fragments of IGFBP-5 in Escherichia coli; the first encodes the N-terminal domain of the protein (residues 1-104) and the second, mini-IGFBP-5, comprises residues Ala40 to Ile92. We show that the entire IGFBP-5 protein contains only one high-affinity binding site for IGFs, located in mini-IGFBP-5. The solution structure of mini-IGFBP-5, determined by nuclear magnetic resonance spectroscopy, discloses a rigid, globular structure that consists of a centrally located three-stranded anti-parallel beta-sheet. Its scaffold is stabilized further by two inside packed disulfide bridges. The binding to IGFs, which is in the nanomolar range, involves conserved Leu and Val residues localized in a hydrophobic patch on the surface of the IGFBP-5 protein. Remarkably, the IGF-I receptor binding assays of IGFBP-5 showed that IGFBP-5 inhibits the binding of IGFs to the IGF-I receptor, resulting in reduction of receptor stimulation and autophosphorylation. Compared with the full-length IGFBP-5, the smaller N-terminal fragments were less efficient inhibitors of the IGF-I receptor binding of IGFs.


==About this Structure==
==About this Structure==
1BOE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BOE OCA].  
1BOE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BOE OCA].  


==Reference==
==Reference==
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[[Category: Georgescu, J.]]
[[Category: Georgescu, J.]]
[[Category: Grol, M.]]
[[Category: Grol, M.]]
[[Category: Holak, T.H.]]
[[Category: Holak, T H.]]
[[Category: Kalus, W.]]
[[Category: Kalus, W.]]
[[Category: Lang, K.]]
[[Category: Lang, K.]]
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[[Category: nmr]]
[[Category: nmr]]


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