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2nou

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(New page: 200px<br /><applet load="2nou" size="450" color="white" frame="true" align="right" spinBox="true" caption="2nou" /> '''Membrane induced structure of Scyliorhinin I...)
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'''Membrane induced structure of Scyliorhinin I: A Dual NK1/NK2 agonist'''<br />
'''Membrane induced structure of Scyliorhinin I: A Dual NK1/NK2 agonist'''<br />
==Overview==
==Overview==
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Scyliorhinin I, a linear decapeptide, is the only known tachykinin that, shows high affinity for both NK-1 and NK-2 binding sites and low affinity, for NK-3 binding sites. As a first step to understand the, structure-activity relationship, we report the membrane-induced structure, of scyliorhinin I with the aid of circular dichroism and 2D-(1)H NMR, spectroscopy. Sequence specific resonance assignments of protons have been, made from correlation spectroscopy (TOCSY, DQF-COSY) and NOESY, spectroscopy. The interproton distance constraints and dihedral angle, constraints have been utilized to generate a family of structures using, DYANA. The superimposition of 20 final structures has been reported with, backbone pairwise root mean-square deviation of 0.38 +/- 0.19 A. The, results show that scyliorhinin I exists in a random coil state in aqueous, environments, whereas helical conformation is induced toward the, C-terminal region of the peptide (D4-M10) in the presence of dodecyl, phosphocholine micelles. Analysis of NMR data is suggestive of the, presence of a 3(10)-helix that is in equilibrium with an alpha-helix in, this region from residue 4 to 10. An extended highly flexible N-terminus, of scyliorhinin I displays some degree of order and a possible turn, structure. Observed conformational features have been compared with, respect to that of substance P and neurokinin A, which are endogenous, agonists of NK-1 and NK-2 receptors, respectively.
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Scyliorhinin I, a linear decapeptide, is the only known tachykinin that shows high affinity for both NK-1 and NK-2 binding sites and low affinity for NK-3 binding sites. As a first step to understand the structure-activity relationship, we report the membrane-induced structure of scyliorhinin I with the aid of circular dichroism and 2D-(1)H NMR spectroscopy. Sequence specific resonance assignments of protons have been made from correlation spectroscopy (TOCSY, DQF-COSY) and NOESY spectroscopy. The interproton distance constraints and dihedral angle constraints have been utilized to generate a family of structures using DYANA. The superimposition of 20 final structures has been reported with backbone pairwise root mean-square deviation of 0.38 +/- 0.19 A. The results show that scyliorhinin I exists in a random coil state in aqueous environments, whereas helical conformation is induced toward the C-terminal region of the peptide (D4-M10) in the presence of dodecyl phosphocholine micelles. Analysis of NMR data is suggestive of the presence of a 3(10)-helix that is in equilibrium with an alpha-helix in this region from residue 4 to 10. An extended highly flexible N-terminus of scyliorhinin I displays some degree of order and a possible turn structure. Observed conformational features have been compared with respect to that of substance P and neurokinin A, which are endogenous agonists of NK-1 and NK-2 receptors, respectively.
==About this Structure==
==About this Structure==
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2NOU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2NOU OCA].
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2NOU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NOU OCA].
==Reference==
==Reference==
Membrane-Induced Structure of Scyliorhinin I: A Dual NK1/NK2 Agonist., Dike A, Cowsik SM, Biophys J. 2005 May;88(5):3592-600. Epub 2005 Feb 24. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15731392 15731392]
Membrane-Induced Structure of Scyliorhinin I: A Dual NK1/NK2 Agonist., Dike A, Cowsik SM, Biophys J. 2005 May;88(5):3592-600. Epub 2005 Feb 24. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15731392 15731392]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Cowsik, S.M.]]
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[[Category: Cowsik, S M.]]
[[Category: Dike, A.]]
[[Category: Dike, A.]]
[[Category: 3-10 helix]]
[[Category: 3-10 helix]]
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[[Category: lipid induced conformation]]
[[Category: lipid induced conformation]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 12:49:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:09:15 2008''

Revision as of 16:09, 21 February 2008


2nou

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Membrane induced structure of Scyliorhinin I: A Dual NK1/NK2 agonist

Overview

Scyliorhinin I, a linear decapeptide, is the only known tachykinin that shows high affinity for both NK-1 and NK-2 binding sites and low affinity for NK-3 binding sites. As a first step to understand the structure-activity relationship, we report the membrane-induced structure of scyliorhinin I with the aid of circular dichroism and 2D-(1)H NMR spectroscopy. Sequence specific resonance assignments of protons have been made from correlation spectroscopy (TOCSY, DQF-COSY) and NOESY spectroscopy. The interproton distance constraints and dihedral angle constraints have been utilized to generate a family of structures using DYANA. The superimposition of 20 final structures has been reported with backbone pairwise root mean-square deviation of 0.38 +/- 0.19 A. The results show that scyliorhinin I exists in a random coil state in aqueous environments, whereas helical conformation is induced toward the C-terminal region of the peptide (D4-M10) in the presence of dodecyl phosphocholine micelles. Analysis of NMR data is suggestive of the presence of a 3(10)-helix that is in equilibrium with an alpha-helix in this region from residue 4 to 10. An extended highly flexible N-terminus of scyliorhinin I displays some degree of order and a possible turn structure. Observed conformational features have been compared with respect to that of substance P and neurokinin A, which are endogenous agonists of NK-1 and NK-2 receptors, respectively.

About this Structure

2NOU is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

Membrane-Induced Structure of Scyliorhinin I: A Dual NK1/NK2 Agonist., Dike A, Cowsik SM, Biophys J. 2005 May;88(5):3592-600. Epub 2005 Feb 24. PMID:15731392

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