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Smartox/Waglerin-1 blocks muscle nAChRs/WAG002-00500/0.5mg

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¥6988.80
货号:WAG002-00500
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品牌:Smartox
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商品描述

Waglerin-1(Wtx-1) isapeptideoriginallyisolatedfromthevenomoftheWagler’spitviper(Trimeresuruswagleri).This22amino-acidpeptideisacompetitiveantagoNISTofadultmusclenicotinicacetylcholinereceptors. Waglerin-1 bindsselectivelytoepsilonsubunitofnAChR.Somestudieshavedemonstratedthat Waglerin-1 hasaneffectonionotropicGABAreceptors.ItmaypotentiateordepressI(GABA)dependingontheneurons.Somederivativesof Waglerin-1 arecurrentlyusedincosmeticstoreducewrinkles.ThefluorescentderivativeWaglerin-1-FAMcanbeusetoexploretheexpressionandfunctionoftheadultnAChRsubtypes.


Description:

Productcode:WAG002.Category:NicotinicAcetylcholineReceptor.Tags:bungarotoxin,nachr,nicotinic.

AAsequence: FAM-Gly-Gly-Lys-Pro-Asp-Leu-Arg-Pro-Cys9-His-Pro-Pro-Cys13-His-Tyr-Ile-Pro-Arg-Pro-Lys-Pro-Arg-OH
Disulfidebonds: Cys9-Cys13
Length(aa): 22
Formula:C133H185N37O32S2
MolecularWeight: 2878.27Da
CASnumber: NA
Source: Synthetic
Fluorescentdye:FAM,5(6)-carboxyfluorescein(λex492,λem517)

Reference:

Peptide-toxintoolsforprobingtheexpressionandfunctionoffetalandadultsubtypesofthenicotinicacetylcholinereceptor

Althoughtheneuromuscularnicotinicacetylcholinereceptor(nAChR)isoneofthemostintensivelystudiedionchannelsinthenervoussystem,thedifferentialrolesoffetalandadultsubtypesofthenAChRundernormalandpathologicalconditionsarestillincompletelydefined.Untilrecently,nopharmacologicaltoolsdistinguishedbetweenfetalandadultsubtypes.Waglerintoxins(fromsnakevenom)&alphaA(S)-conotoxins(fromcone-snailvenom)haveprovidedsuchtools.Becausethesepeptideswerecharacterizedbydifferentresearchgroupsusingdifferentmethods,wehave:1)moreextensivelytestedtheirsubtypeselectivity,and2)beguntoexplorehowthesepeptidesmaybeusedinconcerttoelucidateexpressionpatternsandfunctionsoffetalandadultnAChRs.Inheterologousexpressionsystemsandnativetissues,Waglerin-1&analphaA(S)-conotoxinanalog,alphaA-OIVA[K15N],arehigh-affinity,highlyselectiveinhibitorsoftheadultandfetalmusclenAChRs,respectively.WehaveusedthepeptidesandtheirfluorescentderivativestoexploretheexpressionandfunctionofthefetalandadultnAChRsubtypes.WhilefluorescentderivativesofthesepeptidesindicatedagradualtransitionfromfetaltoadultmusclenAChRsinmiceduringthefirst2weekspostnatal,weunexpectedlyobservedasteepertransitioninfunctionalexpressioninthemousediaphragmmuscleusingelectrophysiology.Asatoolkitofpharmacologicalagentswithcomplementaryspecificity,alphaA-OIVA[K15N]&Waglerin-1shouldhavefurtherutilityindeterminingtherolesoffetal&adultnAChRsubtypesindevelopment,inmaturetissues,andunderpathologicalconditions.

TeichertRW. etal. Peptide-toxintoolsforprobingtheexpressionandfunctionoffetalandadultsubtypesofthenicotinicacetylcholinereceptor. AnnNYAcadSci. PMID: 18567854

ConformationalanalysisofatoxicpeptidefromTrimeresuruswagleriwhichblocksthenicotinicacetylcholinereceptor
The22-residuetoxicpeptide(WTX1)fromthevenomoftheSoutheastAsiansnakeTrimeresuruswaglerihasmultiplesitesofaction,butitslethaleffecthasbeenattributedtoblockingthepostsynapticacetylcholinereceptorattheneuromuscularjunction.The3-dimensionalstructureofWTX1wasstudiedusing2-dimensionalnuclearmagneticresonancespectroscopy,circulardichroism,andcomputersimulations.Inaqueoussolution,WTX1wasshowntohaveextendedandflexIBLe“tails”definedbyashort,rigiddisulfide-bondedloop.Theflexibleregionscanundergostructuralrearrangementwhenmovedfromanaqueoustoalesspolarenvironmentandmaycontributetoitseffectivenessatdifferentreceptorsites.BysubstitutingGlyorPheforHisatposition10,significanteffectsonthedisulfidebondformationand,thereby,theactivityofthepeptidewereobserved.Theseresultssuggestthatevensubtledifferencesinsingleresiduescanhaveprofoundeffectsonthedynamicsoffolding,disulfidebondformation,&activityofthistoxicpeptide.

SellinLC. etal. ConformationalanalysisofatoxicpeptidefromTrimeresuruswagleriwhichblocksthenicotinicacetylcholinereceptor. BiophysJ. 1996. PMID: 8770182

IdentificationofresiduesatthealphaandepsilonsubunitinterfacesmediatingspeciesselectivityofWaglerin-1fornicotinicacetylcholinereceptors
Waglerin-1(Wtx-1)isa22-aminoacidpeptidethatisacompetitiveantagonistofthemusclenicotinicreceptor(nAChR).WefindthatWtx-1binds2100-foldmoretightlytothealpha-epsilonthantothealpha-deltabindingsiteinterfaceofthemousenAChR.Moreover,Wtx-1binds100-foldmoretightlytothealpha-epsiloninterfacefrommousenAChRthanthatfromratorhumansources.Site-directedmutagenesisofresiduesdifferingintheextracellulardomainsofratandmouseepsilonsubunitsindicatesthatresidues59and115mediatethespeciesdifferenceinWtx-1affinity.Mutationofresidues59(Aspinmouse,Gluinratepsilon)and115(Tyrinmouse,Serinratepsilon)convertsWtx-1affinityforthealpha-epsiloninterfaceofonespeciestothatoftheotherspecies.Studiesofdifferentmutationsatposition59indicatebothstericandelectrostaticcontributionstoWtx-1affinity,whereasatposition115,botharomaticandpolargroupscontributetoaffinity.ThehumannAChRalsohasloweraffinityforWtx-1thanmousenAChR,butunlikeratnAChR,residuesinbothalphaandepsilonsubunitsmediatetheaffinitydifference.InhumannAChR,polarresidues(Ser-187andThr-189)conferlowaffinity,whereasinmousenAChRaromaticresidues(Trp-187andPhe-189)conferhighaffinity.Theoverallresultsshowthatnon-conservedresiduesatthenAChRbindingsite,althoughnotcrucialforactivationbyACh,governthepotencyofneuromusculartoxins.

MollesBE. etal. IdentificationofresiduesatthealphaandepsilonsubunitinterfacesmediatingspeciesselectivityofWaglerin-1fornicotinicacetylcholinereceptors. JBiolChem.2002. PMID: 11724791

Waglerin-1selectivelyblockstheepsilonformofthemusclenicotinicacetylcholinereceptor
NeonatalmiceresistthelethaleffectofWaglerin-1.BecauseWaglerin-1blocksthenicotinicacetylcholinereceptorofmatureend-plates,theappearanceoflethalitymayresultfromtheepsilon-forgamma-subunitsubstitution.Insupportofthishypothesis,adultknockout(KO)micelackingthegenecodingfortheepsilon-subunitresistthelethaleffectofWaglerin-1.Incontrast,heterozygouslittermatesrespondtoWaglerin-1likeadultwild-typemice.Invitroapplicationof1microMWaglerin-1inhibitedspontaneousminiatureend-platepotentialsandevokedend-platepotentialsofadultwild-typeandheterozygousKOmice.Bothminiatureend-platepotentialsandend-platepotentialsofneonatalwild-typeandadulthomozygousKOmiceresistedWaglerin-1.Waglerin-1decreasedtheend-plateresponseofadultwild-typemicetoiontophoreticallyappliedacetylcholine(ACh)withanIC50valueof50nM;1microMWaglerin-1decreasedtheAChresponseto4+/-1%ofcontrolforadultheterozygousKOmice.Incontrast,1microMWaglerin-1decreasedtheAChresponseto73+/-2%ofcontrolforwild-typemicelessthan11daysoldandhadnoeffectontheAChresponseofadulthomozygousKOmice.Between11and12daysafterbirth,thesuppressanteffectofWaglerin-1onwild-typeend-plateresponsestoAChdramaticallyincreased.Waglerin-1reducedbindingofalpha-bungarotoxintoend-platesofadultbutnotneonatalwild-typemice.ThesedatademonstratethatWaglerin-1selectivelyblocksthemousemusclenicotinicacetylcholinereceptorcontainingtheepsilon-subunit.

McArdleJJ. etal.Waglerin-1selectivelyblockstheepsilonformofthemusclenicotinicacetylcholinereceptor. JPharmacolExpTher. PMID: 10087048

Waglerin-1inhibitsGABA(A)currentofneuronsinthenucleusaccumbensofneonatalrats.BrainRes

TheeffectofWaglerin-1,a22-aminoacidpeptidepurifiedfromthevenomofWagler’spitviperonthewholecellcurrentresponse(I(GABA))togamma-aminobutyricacid(GABA)wasexaminedforneuronsfreshlyisolatedfromthenucleusaccumbensof3-to7-day-oldrats.Waglerin-1depressedI(GABA)inducedbysubsaturatingconcentrationsofGABA;theIC(50)forI(GABA)inducedby10microMGABAwas2.5microMWaglerin-1.ThisconcentrationofWaglerin-1shiftedtheGABAconcentration-responsecurvetotherightinaparallelmanner,increasingtheGABAEC(50)from12+/-3to27+/-5microM.ThedepressanteffectofWaglerin-1wasgreateratnegativeholdingpotentials.Zn(2+)alsoinhibitedI(GABA)withanIC(50)of0.3microM.PhosphorylationstateappearedtomodulateGABA(A)receptorsensitivitytotheinhibitoryeffectofWaglerin-1sincedialysisofneuronswithN-[2-((p-bromocinnamyl)amino)ethyl]-5-isoquinolinesulfonamideHCl(H-89),aninhibitorofproteinkinaseA,preventedinhibition.ThedataarediscussedintermsofdevelopmentalinfluencesonthesubunitcompositionofGABA(A)receptorsinneuronsofthenucleusaccumbens.

YeJH. etal. Waglerin-1inhibitsGABA(A)currentofneuronsinthenucleusaccumbensofneonatalrats. BrainRes. 1999. PMID: 10433985

Waglerin-1modulatesgamma-aminobutyricacidactivatedcurrentofmurinehypothalamicneurons
WeexaminedtheeffectofWaglerin-1,apeptideof22aminoacidresiduespurifiedfromthevenomofWagler’spitviper(Trimeresuruswagleri),onthewholecellcurrentresponse(I(GABA))offreshlyisolatedmurinehypothalamicneuronstogamma-aminobutyricacid(GABA).Althoughtheapplicationof32microMWaglerin-1alonehadnoeffectonmembraneconductance,coapplicationwithGABAincreasedI(GABA)for78andsuppressedI(GABA)for44ofthe141neuronsexamined.ThepotentiatingeffectofWaglerin-1wasassociatedwithaleftwardshiftoftheconcentration-responserelationofGABAwithoutincreasingpeakI(GABA).ThispotentiatingeffectofWaglerin-1onI(GABA)mimicsdiazepam.FurThermore,thebenzodiazepineantagonistflumazenilantagonizedWaglerin-1potentiationofI(GABA),TheseobservationssuggestthatWaglerin-1actsonthebenzodiazepinesiteofonetypeofGABA(A)receptor/channelcomplextoincreaseitsaffinityforagonist.Incontrast,thedepressanteffectofWaglerin-1wasassociatedwitharightwardshiftoftheconcentration-responserelationofGABAwithoutdepressingthemaximalI(GABA);thissuggestsacompetitiveinhibitionofasecondclassofGABAR.TheABIlityofWaglerin-1tosuppressI(GABA)showedapositivecorrelationwithasimilaractionofZn++.AswithZn++,thedepressanteffectofWaglerin-1onI(GABA)wasmorepronouncedatnegativeholdingpotentials.TheseobservationsarediscussedintermsofvariationinthesubunitcompositionofGABAreceptorsthatmurinecentralnervoussystemneuronsexpress.

YeJH. etal.Waglerin-1modulatesgamma-aminobutyricacidactivatedcurrentofmurinehypothalamicneurons. JPharmacolExpTher. PMID: 9223541 Smartox生物素ProTx-I电压门控钠通道和T型Cav的阻断剂毒素I(ProTx-1;β-theraphotoxin-Tp1a) 是一种毒素,最初是从Prixopelma pruriens(秘鲁绿色天鹅绒狼蛛)的毒液中分离出来的。此毒素可逆地抑制抗河豚毒素(TTX)的通道 Na v 1.8(IC 50  = 27 nM)和 Na v 1.2,Na v 1.5和Na v 1.7  ,IC 50 值为50至100 nM。此外,  ProTx-I 改变了T型Ca v 3.1通道的电压依赖性活动  (IC 50 = 50 nM),而不会影响灭活的电压依赖性。生物素ProTx-I是ProTx-I的生物素标签版本。

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