1kvg

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(New page: 200px<br /><applet load="1kvg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1kvg" /> '''EPO-3 beta Hairpin Peptide'''<br /> ==Overv...)
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'''EPO-3 beta Hairpin Peptide'''<br />
'''EPO-3 beta Hairpin Peptide'''<br />
==Overview==
==Overview==
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Display of peptide libraries on filamentous phage has led to the, identification of peptides of the form X(2-5)CX(2)GPXTWXCX(2-5) (where X, is a variable residue) that bind to the extra-cellular portion of the, erythropoietin receptor (EPO-R). These peptides adopt beta-hairpin, conformations when co-crystallized with EPO-R. Solution NMR studies reveal, that the peptide is conformationally heterogeneous in the absence of, receptor due to cis-trans isomerization about the Gly-Pro peptide bond., Replacement of the conserved threonine residue with glycine at the turn, i+3 position produces a stable beta-hairpin conformation in solution, although this peptide no longer has activity in an EPO-R-dependent cell, proliferation assay. A truncated form of the EPO-R-binding peptide, (containing the i+3 glycine residue) also forms a highly populated, monomeric beta-hairpin. In contrast, phage-derived peptide antagonists of, insulin-like growth factor binding protein 1 (IGFBP-1) have a high level, of sequence identity with the truncated EPO-R peptide (eight of 12, residues) yet adopt a turn-alpha-helix conformation in solution. Peptides, containing all possible pairwise amino acid substitutions between the, EPO-R and IGFBP-1 peptides have been analyzed to assess the degree to, which the non-conserved residues stabilize the hairpin or helix, conformation. All four residues present in the original sequence are, required for maximum population of either the beta-hairpin or alpha-helix, conformation, although some substitutions have a more dominant effect. The, results demonstrate that, within a given sequence, the observed, conformation can be dictated by a small subset of the residues (in this, case four out of 12).
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Display of peptide libraries on filamentous phage has led to the identification of peptides of the form X(2-5)CX(2)GPXTWXCX(2-5) (where X is a variable residue) that bind to the extra-cellular portion of the erythropoietin receptor (EPO-R). These peptides adopt beta-hairpin conformations when co-crystallized with EPO-R. Solution NMR studies reveal that the peptide is conformationally heterogeneous in the absence of receptor due to cis-trans isomerization about the Gly-Pro peptide bond. Replacement of the conserved threonine residue with glycine at the turn i+3 position produces a stable beta-hairpin conformation in solution, although this peptide no longer has activity in an EPO-R-dependent cell proliferation assay. A truncated form of the EPO-R-binding peptide (containing the i+3 glycine residue) also forms a highly populated, monomeric beta-hairpin. In contrast, phage-derived peptide antagonists of insulin-like growth factor binding protein 1 (IGFBP-1) have a high level of sequence identity with the truncated EPO-R peptide (eight of 12 residues) yet adopt a turn-alpha-helix conformation in solution. Peptides containing all possible pairwise amino acid substitutions between the EPO-R and IGFBP-1 peptides have been analyzed to assess the degree to which the non-conserved residues stabilize the hairpin or helix conformation. All four residues present in the original sequence are required for maximum population of either the beta-hairpin or alpha-helix conformation, although some substitutions have a more dominant effect. The results demonstrate that, within a given sequence, the observed conformation can be dictated by a small subset of the residues (in this case four out of 12).
==About this Structure==
==About this Structure==
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1KVG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with NH2 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1KVG OCA].
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1KVG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=NH2:'>NH2</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KVG OCA].
==Reference==
==Reference==
Amino acid determinants of beta-hairpin conformation in erythropoeitin receptor agonist peptides derived from a phage display library., Skelton NJ, Russell S, de Sauvage F, Cochran AG, J Mol Biol. 2002 Mar 8;316(5):1111-25. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11884148 11884148]
Amino acid determinants of beta-hairpin conformation in erythropoeitin receptor agonist peptides derived from a phage display library., Skelton NJ, Russell S, de Sauvage F, Cochran AG, J Mol Biol. 2002 Mar 8;316(5):1111-25. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11884148 11884148]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Cochran, A.G.]]
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[[Category: Cochran, A G.]]
[[Category: Russell, S.]]
[[Category: Russell, S.]]
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[[Category: Sauvage, F.de.]]
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[[Category: Sauvage, F de.]]
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[[Category: Skelton, N.J.]]
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[[Category: Skelton, N J.]]
[[Category: NH2]]
[[Category: NH2]]
[[Category: beta hairpin peptide]]
[[Category: beta hairpin peptide]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:01:21 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:38:20 2008''

Revision as of 11:38, 21 February 2008


1kvg

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EPO-3 beta Hairpin Peptide

Overview

Display of peptide libraries on filamentous phage has led to the identification of peptides of the form X(2-5)CX(2)GPXTWXCX(2-5) (where X is a variable residue) that bind to the extra-cellular portion of the erythropoietin receptor (EPO-R). These peptides adopt beta-hairpin conformations when co-crystallized with EPO-R. Solution NMR studies reveal that the peptide is conformationally heterogeneous in the absence of receptor due to cis-trans isomerization about the Gly-Pro peptide bond. Replacement of the conserved threonine residue with glycine at the turn i+3 position produces a stable beta-hairpin conformation in solution, although this peptide no longer has activity in an EPO-R-dependent cell proliferation assay. A truncated form of the EPO-R-binding peptide (containing the i+3 glycine residue) also forms a highly populated, monomeric beta-hairpin. In contrast, phage-derived peptide antagonists of insulin-like growth factor binding protein 1 (IGFBP-1) have a high level of sequence identity with the truncated EPO-R peptide (eight of 12 residues) yet adopt a turn-alpha-helix conformation in solution. Peptides containing all possible pairwise amino acid substitutions between the EPO-R and IGFBP-1 peptides have been analyzed to assess the degree to which the non-conserved residues stabilize the hairpin or helix conformation. All four residues present in the original sequence are required for maximum population of either the beta-hairpin or alpha-helix conformation, although some substitutions have a more dominant effect. The results demonstrate that, within a given sequence, the observed conformation can be dictated by a small subset of the residues (in this case four out of 12).

About this Structure

1KVG is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

Amino acid determinants of beta-hairpin conformation in erythropoeitin receptor agonist peptides derived from a phage display library., Skelton NJ, Russell S, de Sauvage F, Cochran AG, J Mol Biol. 2002 Mar 8;316(5):1111-25. PMID:11884148

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