1tr6

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(New page: 200px<br /><applet load="1tr6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1tr6" /> '''NMR solution structure of omega-conotoxin [K...)
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'''NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide'''<br />
'''NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide'''<br />
==Overview==
==Overview==
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The omega-conotoxins from fish-hunting cone snails are potent inhibitors, of voltage-gated calcium channels. The omega-conotoxins MVIIA and CVID are, selective N-type calcium channel inhibitors with potential in the, treatment of chronic pain. The beta and alpha(2)delta-1 auxiliary subunits, influence the expression and characteristics of the alpha(1B) subunit of, N-type channels and are differentially regulated in disease states, including pain. In this study, we examined the influence of these, auxiliary subunits on the ability of the omega-conotoxins GVIA, MVIIA, CVID and analogues to inhibit peripheral and central forms of the rat, N-type channels. Although the beta3 subunit had little influence on the, on- and off-rates of omega-conotoxins, coexpression of alpha(2)delta with, alpha(1B) significantly reduced on-rates and equilibrium inhibition at, both the central and peripheral isoforms of the N-type channels. The, alpha(2)delta also enhanced the selectivity of MVIIA, but not CVID, for, the central isoform. Similar but less pronounced trends were also observed, for N-type channels expressed in human embryonic kidney cells. The, influence of alpha(2)delta was not affected by oocyte deglycosylation. The, extent of recovery from the omega-conotoxin block was least for GVIA, intermediate for MVIIA, and almost complete for CVID. Application of a, hyperpolarizing holding potential (-120 mV) did not significantly enhance, the extent of CVID recovery. Interestingly, [R10K]MVIIA and [O10K]GVIA had, greater recovery from the block, whereas [K10R]CVID had reduced recovery, from the block, indicating that position 10 had an important influence on, the extent of omega-conotoxin reversibility. Recovery from CVID block was, reduced in the presence of alpha(2)delta in human embryonic kidney cells, and in oocytes expressing alpha(1B-b). These results may have implications, for the antinociceptive properties of omega-conotoxins, given that the, alpha(2)delta subunit is up-regulated in certain pain states.
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The omega-conotoxins from fish-hunting cone snails are potent inhibitors of voltage-gated calcium channels. The omega-conotoxins MVIIA and CVID are selective N-type calcium channel inhibitors with potential in the treatment of chronic pain. The beta and alpha(2)delta-1 auxiliary subunits influence the expression and characteristics of the alpha(1B) subunit of N-type channels and are differentially regulated in disease states, including pain. In this study, we examined the influence of these auxiliary subunits on the ability of the omega-conotoxins GVIA, MVIIA, CVID and analogues to inhibit peripheral and central forms of the rat N-type channels. Although the beta3 subunit had little influence on the on- and off-rates of omega-conotoxins, coexpression of alpha(2)delta with alpha(1B) significantly reduced on-rates and equilibrium inhibition at both the central and peripheral isoforms of the N-type channels. The alpha(2)delta also enhanced the selectivity of MVIIA, but not CVID, for the central isoform. Similar but less pronounced trends were also observed for N-type channels expressed in human embryonic kidney cells. The influence of alpha(2)delta was not affected by oocyte deglycosylation. The extent of recovery from the omega-conotoxin block was least for GVIA, intermediate for MVIIA, and almost complete for CVID. Application of a hyperpolarizing holding potential (-120 mV) did not significantly enhance the extent of CVID recovery. Interestingly, [R10K]MVIIA and [O10K]GVIA had greater recovery from the block, whereas [K10R]CVID had reduced recovery from the block, indicating that position 10 had an important influence on the extent of omega-conotoxin reversibility. Recovery from CVID block was reduced in the presence of alpha(2)delta in human embryonic kidney cells and in oocytes expressing alpha(1B-b). These results may have implications for the antinociceptive properties of omega-conotoxins, given that the alpha(2)delta subunit is up-regulated in certain pain states.
==About this Structure==
==About this Structure==
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1TR6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Conus_geographus Conus geographus] 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=1TR6 OCA].
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1TR6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Conus_geographus Conus geographus] 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=1TR6 OCA].
==Reference==
==Reference==
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[[Category: Conus geographus]]
[[Category: Conus geographus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Adams, D.J.]]
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[[Category: Adams, D J.]]
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[[Category: Beedle, A.M.]]
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[[Category: Beedle, A M.]]
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[[Category: Doering, C.J.]]
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[[Category: Doering, C J.]]
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[[Category: Lewis, R.J.]]
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[[Category: Lewis, R J.]]
[[Category: Mould, J.]]
[[Category: Mould, J.]]
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[[Category: Schroeder, C.I.]]
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[[Category: Schroeder, C I.]]
[[Category: Yasuda, T.]]
[[Category: Yasuda, T.]]
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[[Category: Zamponi, G.W.]]
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[[Category: Zamponi, G W.]]
[[Category: NH2]]
[[Category: NH2]]
[[Category: cysteine knot]]
[[Category: cysteine knot]]
[[Category: four-loop frame work]]
[[Category: four-loop frame work]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 03:31:41 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:16:33 2008''

Revision as of 13:16, 21 February 2008


1tr6

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NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide

Overview

The omega-conotoxins from fish-hunting cone snails are potent inhibitors of voltage-gated calcium channels. The omega-conotoxins MVIIA and CVID are selective N-type calcium channel inhibitors with potential in the treatment of chronic pain. The beta and alpha(2)delta-1 auxiliary subunits influence the expression and characteristics of the alpha(1B) subunit of N-type channels and are differentially regulated in disease states, including pain. In this study, we examined the influence of these auxiliary subunits on the ability of the omega-conotoxins GVIA, MVIIA, CVID and analogues to inhibit peripheral and central forms of the rat N-type channels. Although the beta3 subunit had little influence on the on- and off-rates of omega-conotoxins, coexpression of alpha(2)delta with alpha(1B) significantly reduced on-rates and equilibrium inhibition at both the central and peripheral isoforms of the N-type channels. The alpha(2)delta also enhanced the selectivity of MVIIA, but not CVID, for the central isoform. Similar but less pronounced trends were also observed for N-type channels expressed in human embryonic kidney cells. The influence of alpha(2)delta was not affected by oocyte deglycosylation. The extent of recovery from the omega-conotoxin block was least for GVIA, intermediate for MVIIA, and almost complete for CVID. Application of a hyperpolarizing holding potential (-120 mV) did not significantly enhance the extent of CVID recovery. Interestingly, [R10K]MVIIA and [O10K]GVIA had greater recovery from the block, whereas [K10R]CVID had reduced recovery from the block, indicating that position 10 had an important influence on the extent of omega-conotoxin reversibility. Recovery from CVID block was reduced in the presence of alpha(2)delta in human embryonic kidney cells and in oocytes expressing alpha(1B-b). These results may have implications for the antinociceptive properties of omega-conotoxins, given that the alpha(2)delta subunit is up-regulated in certain pain states.

About this Structure

1TR6 is a Single protein structure of sequence from Conus geographus with as ligand. Full crystallographic information is available from OCA.

Reference

The alpha2delta auxiliary subunit reduces affinity of omega-conotoxins for recombinant N-type (Cav2.2) calcium channels., Mould J, Yasuda T, Schroeder CI, Beedle AM, Doering CJ, Zamponi GW, Adams DJ, Lewis RJ, J Biol Chem. 2004 Aug 13;279(33):34705-14. Epub 2004 May 27. PMID:15166237

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