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Smartox/Selective blocker of SK2 (KCa2.2) channels/10TAM001-00500/0.5mg
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Tamapin isapeptidetoxinisolatedfromthevenomoftheIndianredscorpionMesobuthusTamulus. Tamapin isamidatedatitsC-terminaltyrosineresidue. Tamapin bindsto smallconductanceCa2+-activatedK+ channels(SKchannels) withhighaffinityandinhibitsSKchannel-mediatedcurrentsinpyramidalneuronsofthehippocampusaswellasincelllinesexpressingdistinctSKchannelsubunits.Contraryto Apamin or Leiurotoxin-1(Scyllatoxin), Tamapin isanexcellenttoxintodiscriminateamongSKchannelsubtypesbecauseitpresentsdifferentaffinitiesfor SK1(42nM),SK2(24pM)andSK3(1.7nM) channels.ThistoxinisalsothemostpotentSK2channelblockercharacterizedsofar(IC50 forSK2channels=24pM).Description:Productcode:N/A.Categories:KCachannels,Potassiumchannels.Tag:SK.AAsequence: Ala-Phe-Cys3-Asn-Leu-Arg-Arg-Cys8-Glu-Leu-Ser-Cys12-Arg-Ser-Leu-Gly-Leu-Leu-Gly-Lys-Cys21-Ile-Gly-Glu-Glu-Cys26-Lys-Cys28-Val-Pro-Tyr-NH2Disulfidebridges: Cys3-Cys21;Cys8-Cys26;Cys12-Cys28Length(aa): 31Formula: C146H237N44O41S6MolecularWeight: 3459.00DaAppearance: WhitelyophilizedsolidSolubility: waterandsalinebufferCASnumber: notavailableSource: SyntheticPurityrate: >97%Reference:SmallconductanceCa2+-activatedK+channelsastargetsofCNSdrugdevelopmentInmostcentralneurons,smallconductanceCa(2+)-activatedK(+)channels(SKchannels)contributetoafterhyperpolarizations(AHPs),whichcontrolneuronalexcitABIlity.ThemediumAHPhaspharmacologicalpropertiessimilartorecombinantSKchannels,consistentwiththehypothesisthatSKchannelsgeneratethisafterhyperpolarizationcomponent.ItisstillunclearhowrecombinantSKchannelsarefunctionallyrelatedtotheslowAHPcomponent.ClonedSKchannelsareheteromericcomplexesofSKchannelsubunitsandcalmodulin.ThechannelsareactivatedbyCa(2+)bindingtocalmodulinthatinducesconformationalchangesresultinginchannelopening.ChanneldeactivationisthereverseprocessbroughtaboutbydissociationofCa(2+)fromcalmodulin.Inthemammalianbrain,thethreeSKchannelsubunits(SK1-3)displaypartiallyoverlappingdistributions.MostofthehigherbrainregionssuchastheneocortexandhippocampusshowexpressionofbothgenesencodingSK1andSK2channels,whereasphylogeneticallyolderbrainregionssuchasthethalamus,basalganglia,cerebellum,andbrainstemshowhighlevelsofSK3geneexpression.Atpresent,itisstillunclearwhethernativeSKchannelsaregeneratedasheteromericorhomomericchannels.Peptidetoxinssuchasapaminandscyllatoxin,aswellasorganiccompoundssuchasquaternarysaltsofbicuculline,dequalinium,UCL1684andUCL1848serveasnon-specificSKchannelblockers.TheonlyknownexceptionssofararethescorpiontoxintamapinandthepeptideinhibitorLei-Dab(7),whichbindpreferentiallytoSK2.ElectrophysiologicalandbehavioralstudiesindicatethatblockadeofSKchannelsbyapaminincreasesexcitability,lowersthethresholdfortheinductionofsynapticplasticity,andfacilitateshippocampus-dependentmemory.ThepotentialvalueofpharmacologicalSKchannelmodulationinvariouspathologicalstatessuchasincreasedepileptiformactivity,cognitiveimpairment,pain,mooddisordersandschizophreniawillbediscussed.BlankT., etal. (2004)SmallconductanceCa2+-activatedK+channelsastargetsofCNSdrugdevelopment. CurrDrugTargetsCNSNeurolDisord. PMID: 15180477Tamapin,avenompeptidefromtheIndianredscorpion(Mesobuthustamulus)thattargetssmallconductanceCa2+-activatedK+channelsandafterhyperpolarizationcurrentsincentralneuronsThebiophysicalpropertiesofsmallconductanceCa(2+)-activatedK(+)(SK)channelsarewellsuitedtounderlieafterhyperpolarizations(AHPs)shapingthefiringpatternsofaconspicuousnumberofcentralandperipheralneurons.Wehaveidentifiedanewscorpiontoxin(tamapin)thatbindstoSKchannelswithhighaffinityandinhibitsSKchannel-mediatedcurrentsinpyramidalneuronsofthehippocampusaswellasincelllinesexpressingdistinctSKchannelsubunits.ThistoxindistinguishedbetweentheSKchannelsunderlyingtheapamin-sensitiveI(AHP)andtheCa(2+)-activatedK(+)channelsmediatingtheslowI(AHP)(sI(AHP))inhippocampalneurons.Comparedwithrelatedscorpiontoxins,tamapindisplayedaunique,remarkableselectivityforSK2versusSK1(approximately1750-fold)andSK3(approximately70-fold)channelsandisthemostpotentSK2channelblockercharacterizedsofar(IC(50)forSK2channels=24pm).TamapinwillfacilitatethecharacterizationofthesubunitcompositionofnativeSKchannelsandhelpdeterminetheirinvolvementinelectricalandbiochemicalsignaling.PedarzaniP etal. (2002)Tamapin,avenompeptidefromtheIndianredscorpion(Mesobuthustamulus)thattargetssmallconductanceCa2+-activatedK+ channelsandafterhyperpolarizationcurrentsincentralneurons. J.BiolChem. PMID: 12239213

Smartox Biotechnology 是全球唯一一家专门生产动物毒液多肽毒素,用于细胞离子通道功能研究的生物医药公司。多肽毒素在生物制药领域具有重要的使用价值。Smartox Biotechnology 于 2009 年由来自 Grenoble 神经科学研究所 (Grenoble Institute of Neuroscience) 的 Michel de waard 博士创立, Smartox Biotechnology 专门研究动物毒液,制作合成多种毒液中的多肽成分(常称为毒素)。 De Waard 博士研究离子通道与毒素多肽的关系,尤其是鉴定、开发毒素多肽作为治疗性分子或细胞穿透肽 (cell penetrating peptides, CPP) 。其研究团队在毒液分离,药理性活性肽鉴定、富半胱氨酸肽定性、制作和优化等方面具有独特、丰富的经验。 2010 年, Smartox Biotechnolgy 被法国研究部 (Ministry of Research) 授予“新兴企业 OSEO 奖 (OSEO prize for emerging businesses) ”。 

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