Formulation | 25mMHepes,150mMNaCl,pH7.4 |
Storage | -80°C |
Purity | >95%bySDS-PAGE |
ActivityDetermination | N/A |
ShelfLife(properlystored) | 12months |
Gel | Novex4-12%Bis-Tris |
---|---|
Load | Load:HumanBetaThromboglobulin,1µgperlane |
Buffer | MES |
Standard | SeeBluePlus2;Myosin(188kDa),PhosphorylaseB(98kDa),BSA(62kDa),GlutamicDehydrogenase(49kDa),AlcoholDehydrogenase(38kDa),CarbonicAnhydrase(28kDa),MyoglobinRed(17kDa),Lysozyme(14kDa),Aprotinin(6kDa),Insulin,Bchain(3kDa). |
β-thromboglobulin(b-TG),isalowmolecularweight,heparin-binding,platelet-derivedprotein(1).Itissimilartoplateletfactor-4(PF-4)inthatitislocalizedwithintheplateletalpha-granuleatlevelsreportedtorangefrom8.1-24.2µgper109platelets(2,3).Therelativeconcentrationofβ-TGinplateletsexceedsthatofplasmaby260,000-fold(4)makingβ-TGaconvenientMarkerofplateletactivation.Structurally,β-TGisanalogoustoPF-4inthat,initsnativestate,β-TGisatetramer(1)consistingoffouridentical8800molecularweightpeptidechains(5).IncontrasttoPF-4,β-TGexhibitsaloweraffinityforheparinandalsoexistsasalargermolecularweightspeciesknownas"lowaffinityPF-4"(LAPF-4)(2).β-TGisderivedfromtheproteolyticremovaloffourNH2-terminalaminoacidresiduesfromaLAPF-4(6,7).Immunologicalscreeningofpartiallyfractionatedsupernatantfromactivatedplateletsrevealedahighlybasicformofβ-TGdistinctfromLAPF-4(7).Thisbasicβ-TGspecies,termedplateletbasicprotein(PBP),wassubsequentlyisolated(8)andlaterconcludedfromimmunological,peptidesequencing,andproteolyticprocessingstudiestobeahighermolecularweightprecursorformofbothLAPF-4andβ-TG(9,10).
Thephysiologicalfunctionofβ-TGisnotknown.Whileearlystudiessuggestedthattheprecursorformsofβ-TGweremitogenicformousefibroblasts(8,11),itwaslaterconcludedthatthisactivitywasduetogrowthfactorcontamination(10).β-TGhasalsobeenreportedtoinhibitprostacyclin-I2productionbyendothelialcells(12),however,therelevanceofthiseffecthasbeencalledintoquestion(13,14).Thechemotacticactivityofplateletalpha-granuleproteinsforhumanfibroblastshasbeenattributedtobothPF-4andβ-TG(15).
Humanβ-TGispreparedfromthesupernatantofactivatedplateletsbyheparin-agaroseaffinitychromatographyandgelfiltration(1,2).Thepurifiedproteinissuppliedin25mMHepes,150mMNaClpH7.4andshouldbestoredat-80°C.PurityisassessedbySDS-PAGEanalysis.
Localization | plateletalpha-granule(3) | |||||
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PlasmaConcentration | 100-200µg/ml | |||||
Modeofaction | heparin-bindingprotein:Plasmaconcentrationusedasamarkerofplateletactivation | |||||
Molecularweight | 35,800(1) | |||||
Extinctioncoefficient |
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Structure | homotetramer(monomer,Mr~8800)(5) |
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