کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1217327 967085 2006 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Simple affinity chromatographic procedure to purify β-galactoside binding lectins
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Simple affinity chromatographic procedure to purify β-galactoside binding lectins
چکیده انگلیسی

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.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography B - Volume 838, Issue 2, 11 July 2006, Pages 135–138
نویسندگان
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