Title of article :
Simple affinity chromatographic procedure to purify β-galactoside binding lectins
Author/Authors :
De-Simone، نويسنده , , S.G. and Netto، نويسنده , , C.C. and Silva Jr.، نويسنده , , F.P.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Abstract :
Affinity chromatography based on the commercial resin Sepharose CL-6B was used to isolate new C1-β-type lectins from crude preparations of snake venoms (Bothrops jararaca, Bothrops jararacussu, Bothrops newiedi, Bothrops moojeni, Lachesis muta rhombeata). Most of the C-type lectins could be eluted with almost 100% recovery using the competitor isopropyl-β-d-thiogalactoside (IPTG) or through Ca2+ sequestration with EDTA. The lectin yield varied considerably among the different snake species, but B. newiedi venom was a particularly rich source of lectin, retaining 2.7 mg of lectin by milliliter of resin in saturating conditions. C1-α-lectins from Crotalus durisus terrificus venom, from the jack fruit (jacalin) and from bread fruit seeds extract (frutalin) had no affinity, either with or without Ca2+ added, for Sepharose CL-6B, showing that the resin is specific for C1-β-type lectins. Sepharose CL-6B used as galactose-affinity chromatography provides a simple and fast method for isolating C-type β-galactoside binding lectins from crude sample preparations.
Keywords :
affinity chromatography , C-type ?-galactoside binding lectins , Lectins
Journal title :
Journal of Chromatography B
Journal title :
Journal of Chromatography B