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2dsr

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{{STRUCTURE_2dsr| PDB=2dsr | SCENE= }}
{{STRUCTURE_2dsr| PDB=2dsr | SCENE= }}
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'''Structural Basis for the Inhibition of Insulin-like Growth Factors by IGF Binding Proteins'''
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===Structural Basis for the Inhibition of Insulin-like Growth Factors by IGF Binding Proteins===
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==Overview==
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Insulin-like growth factor-binding proteins (IGFBPs) control bioavailability, activity, and distribution of insulin-like growth factor (IGF)1 and -2 through high-affinity IGFBP/IGF complexes. IGF-binding sites are found on N- and C-terminal fragments of IGFBPs, the two conserved domains of IGFBPs. The relative contributions of these domains to IGFBP/IGF complexation has been difficult to analyze, in part, because of the lack of appropriate three-dimensional structures. To analyze the effects of N- and C-terminal domain interactions, we determined several x-ray structures: first, of a ternary complex of N- and C-terminal domain fragments of IGFBP4 and IGF1 and second, of a "hybrid" ternary complex using the C-terminal domain fragment of IGFBP1 instead of IGFBP4. We also solved the binary complex of the N-terminal domains of IGFBP4 and IGF1, again to analyze C- and N-terminal domain interactions by comparison with the ternary complexes. The structures reveal the mechanisms of IGF signaling regulation via IGFBP binding. This finding supports research into the design of IGFBP variants as therapeutic IGF inhibitors for diseases of IGF disregulation. In IGFBP4, residues 1-38 form a rigid disulphide bond ladder-like structure, and the first five N-terminal residues bind to IGF and partially mask IGF residues responsible for the type 1 IGF receptor binding. A high-affinity IGF1-binding site is located in a globular structure between residues 39 and 82. Although the C-terminal domains do not form stable binary complexes with either IGF1 or the N-terminal domain of IGFBP4, in the ternary complex, the C-terminal domain contacts both and contributes to blocking of the IGF1 receptor-binding region of IGF1.
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(as it appears on PubMed at http://www.pubmed.gov), where 16924115 is the PubMed ID number.
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{{ABSTRACT_PUBMED_16924115}}
==About this Structure==
==About this Structure==
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[[Category: Igfbp]]
[[Category: Igfbp]]
[[Category: Insulin]]
[[Category: Insulin]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 20:46:23 2008''

Revision as of 17:46, 27 July 2008

Image:2dsr.png

Template:STRUCTURE 2dsr

Structural Basis for the Inhibition of Insulin-like Growth Factors by IGF Binding Proteins

Template:ABSTRACT PUBMED 16924115

About this Structure

2DSR is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural basis for the inhibition of insulin-like growth factors by insulin-like growth factor-binding proteins., Sitar T, Popowicz GM, Siwanowicz I, Huber R, Holak TA, Proc Natl Acad Sci U S A. 2006 Aug 29;103(35):13028-33. Epub 2006 Aug 21. PMID:16924115

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