Article
Simple affinity chromatographic procedure to purify beta-galactoside binding lectins
Registro en:
DE SIMONE, S. G. de; NETTO, C. C.; SILVA JR., F. P. Simple affinity chromatographic procedure to purify -galactoside binding lectins. Journal of Chromotherapy B, v. 838, p. 135-138, 2006.
1570-0232
10.1016/j.jchromb.2006.02.036
Autor
De Simone, S. G.
Netto, C. C.
Silva, F. P.
Resumen
Affinity chromatography based on the commercial resin Sepharose CL-6B was used to isolate new C1-beta-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-beta-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-alpha-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-beta-type lectins. Sepharose CL-6B used as galactose-affinity chromatography provides a simple and fast method for isolating C-type beta-galactoside binding lectins from crude sample preparations. 2022-01-01