کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1953341 1057267 2006 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Purification of a post-synaptic neurotoxic phospholipase A2 from Naja naja venom and its inhibition by a glycoprotein from Withania somnifera
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Purification of a post-synaptic neurotoxic phospholipase A2 from Naja naja venom and its inhibition by a glycoprotein from Withania somnifera
چکیده انگلیسی

A post-synaptic neurotoxic phospholipase A2 (PLA2) has been purified from Indian cobra Naja naja venom. It was associated with a peptide in the venom. The association was disrupted using 8 M urea. It is denoted to be a basic protein by its behavior on both ion exchange chromatography and electrophoresis. It is toxic to mice, LD50 1.9 mg/kg body weight (ip). It is proved to be post-synaptic PLA2 by chymographic experiment using frog nerve-muscle preparation. A glycoprotein, (WSG) was isolated from a folk medicinal plant Withania somnifera. The WSG inhibited the phospholipase A2 activity of NN-XIa-PLA2, isolated from the cobra venom, completely at a mole-to-mole ratio of 1:2 (NN-XIa-PLA2: WSG) but failed to neutralize the toxicity of the molecule. However, it reduced the toxicity as well as prolonged the death time of the experimental mice approximately 10 times when compared to venom alone. The WSG also inhibited several other PLA2 isoforms from the venom to varying extent. The interaction of the WSG with the PLA2 is confirmed by fluorescence quenching and gel-permeation chromatography. Chemical modification of the active histidine residue of PLA2 using p-brophenacyl bromide resulted in the loss of both catalytic activity as well as neurotoxicity of the molecule. These findings suggest that the venom PLA2 has multiple sites on it; perhaps some of them are overlapping. Application of the plant extract on snakebite wound confirms the medicinal value associated with the plant.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimie - Volume 88, Issue 6, June 2006, Pages 701–710
نویسندگان
, ,