Related ArticlesA novel potassium channel blocking toxin from the scorpion Pandinus imperator: A 1H NMR analysis using a nano-NMR probe.
Biochemistry. 1997 Mar 4;36(9):2649-58
Authors: Delepierre M, Prochnicka-Chalufour A, Possani LD
The three-dimensional solution structure of a novel peptide, Pi 1, purified from the venom of the scorpion Pandinus imperator and specific for potassium channels was determined by homonuclear proton NMR methods at 500 MHz from nanomole amounts of compound. P. imperator toxin is a voltage-dependent potassium channel specific peptide capable of blocking the shaker B K+ channels expressed in Sf9 cells in culture (Spodoptera frugiperda cell line no. 9) and displacing labeled noxiustoxin from rat brain synaptosomal membranes. The toxin has only 35 amino acid residues but is stabilized by four disulfide bridges (Cys4-Cys25, Cys10-Cys30, Cys14-Cys32, and Cys20-Cys35) instead of three commonly found in small potassium channel toxins. A detailed nuclear magnetic resonance structure of this protein was obtained using a nano-NMR probe and a combination of two-dimensional proton NMR experiments. The dihedral angles and distance restraints obtained from measured NMR parameters were used in structural calculations in order to determine the solution conformation of the toxin. The structure is organized around a short alpha-helix spanning residues Ser8-Thr18 and a beta-sheet. These two elements of secondary structure are stabilized by two disulfide bridges, Cys10-Cys30 and Cys14-Cys32. The antiparallel beta-sheet is composed of two strands extending from Asn22 to Cys32 with a tight turn at Arg28-Met29 in contact with the N-terminal fragment Leu1-Cys4. Comparison between the 3D structure of Pi 1 and those of other structurally and functionally related scorpion toxins is presented.
[NMR paper] New carbohydrate specificity and HIV-1 fusion blocking activity of the cyanobacterial
New carbohydrate specificity and HIV-1 fusion blocking activity of the cyanobacterial protein MVL: NMR, ITC and sedimentation equilibrium studies.
Related Articles New carbohydrate specificity and HIV-1 fusion blocking activity of the cyanobacterial protein MVL: NMR, ITC and sedimentation equilibrium studies.
J Mol Biol. 2004 Jun 11;339(4):901-14
Authors: Bewley CA, Cai M, Ray S, Ghirlando R, Yamaguchi M, Muramoto K
Carbohydrate-binding proteins that bind their carbohydrate ligands with high affinity are rare and therefore of interest because...
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[NMR paper] NMR detection of slow conformational dynamics in an endonuclease toxin.
NMR detection of slow conformational dynamics in an endonuclease toxin.
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J Biomol NMR. 1998 Jul;12(1):145-59
Authors: Whittaker SB, Boetzel R, MacDonald C, Lian LY, Pommer AJ, Reilly A, James R, Kleanthous C, Moore GR
The cytotoxic activity of the secreted bacterial toxin colicin E9 is due to a non-specific DNase housed in the C-terminus of the protein. Double-resonance and triple-resonance NMR studies of the 134-amino acid 15N- and 13C/15N-labelled DNase...
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[NMR thesis] NMR study of fluoride ion diffusion in potassium-doped ?-PbF_2
NMR study of fluoride ion diffusion in potassium-doped ?-PbF_2
Cannon, David M. (1978) NMR study of fluoride ion diffusion in potassium-doped ?-PbF_2. Master's thesis, California Institute of Technology. http://resolver.caltech.edu/CaltechTHESIS:03292010-111321744
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[NMR paper] A novel potassium channel blocking toxin from the scorpion Pandinus imperator: A 1H N
A novel potassium channel blocking toxin from the scorpion Pandinus imperator: A 1H NMR analysis using a nano-NMR probe.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-acspubs.jpg Related Articles A novel potassium channel blocking toxin from the scorpion Pandinus imperator: A 1H NMR analysis using a nano-NMR probe.
Biochemistry. 1997 Mar 4;36(9):2649-58
Authors: Delepierre M, Prochnicka-Chalufour A, Possani LD
The three-dimensional solution structure of a novel peptide, Pi 1, purified from the venom of the...
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08-22-2010 03:31 PM
[NMR paper] NMR structure of inactivation gates from mammalian voltage-dependent potassium channe
NMR structure of inactivation gates from mammalian voltage-dependent potassium channels.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www.nature.com-images-lo_nature.gif Related Articles NMR structure of inactivation gates from mammalian voltage-dependent potassium channels.
Nature. 1997 Jan 16;385(6613):272-5
Authors: Antz C, Geyer M, Fakler B, Schott MK, Guy HR, Frank R, Ruppersberg JP, Kalbitzer HR
The electrical signalling properties of neurons originate largely from the gating properties of their ion channels. N-type...
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08-22-2010 03:31 PM
[NMR paper] NMR structure of inactivation gates from mammalian voltage-dependent potassium channe
NMR structure of inactivation gates from mammalian voltage-dependent potassium channels.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www.nature.com-images-lo_nature.gif Related Articles NMR structure of inactivation gates from mammalian voltage-dependent potassium channels.
Nature. 1997 Jan 16;385(6613):272-5
Authors: Antz C, Geyer M, Fakler B, Schott MK, Guy HR, Frank R, Ruppersberg JP, Kalbitzer HR
The electrical signalling properties of neurons originate largely from the gating properties of their ion channels. N-type...
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08-22-2010 03:03 PM
[NMR paper] Three-dimensional structure of the RGD-containing snake toxin albolabrin in solution,
Three-dimensional structure of the RGD-containing snake toxin albolabrin in solution, based on 1H NMR spectroscopy and simulated annealing calculations.
Related Articles Three-dimensional structure of the RGD-containing snake toxin albolabrin in solution, based on 1H NMR spectroscopy and simulated annealing calculations.
Int J Pept Protein Res. 1996 Sep;48(3):220-8
Authors: Smith KJ, Jaseja M, Lu X, Williams JA, Hyde EI, Trayer IP
Albolabrin is a snake toxin that contains a RGD-(Arg-Gly-Asp) sequence motif and competes with fibrinogen to bind...
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08-22-2010 02:20 PM
[NMR paper] NMR sequential assignments and solution structure of chlorotoxin, a small scorpion to
NMR sequential assignments and solution structure of chlorotoxin, a small scorpion toxin that blocks chloride channels.
Related Articles NMR sequential assignments and solution structure of chlorotoxin, a small scorpion toxin that blocks chloride channels.
Biochemistry. 1995 Jan 10;34(1):13-21
Authors: Lippens G, Najib J, Wodak SJ, Tartar A
The solution structure of chlorotoxin, a small toxin purified from the venom of the Leiurus quinquestriatus scorpion, has been determined using 2D 1H NMR spectroscopy. Analysis of the NMR data shows that...