1tr6

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[[Image:1tr6.jpg|left|200px]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1tr6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1tr6 OCA], [http://www.ebi.ac.uk/pdbsum/1tr6 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1tr6 RCSB]</span>
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'''NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide'''
'''NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide'''
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[[Category: Yasuda, T.]]
[[Category: Yasuda, T.]]
[[Category: Zamponi, G W.]]
[[Category: Zamponi, G W.]]
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[[Category: cysteine knot]]
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[[Category: Cysteine knot]]
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[[Category: four-loop frame work]]
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Revision as of 07:16, 3 May 2008

Template:STRUCTURE 1tr6

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. 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 Page seeded by OCA on Sat May 3 10:16:39 2008

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