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Proteomic analysis and antivenomics study of Western India Naja naja venom: correlation between venom composition and clinical manifestations of cobra bite in this region

机译:印度西部Naja Naja毒液的蛋白质组学分析与抗动因子研究:该地区眼镜蛇咬伤与临床表现的相关性

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Background: Snakebite is a severe problem in the tropical countries including Indian subcontinent. Premier cases of cobra bites are being reported from western India (WI). Research design and methods: The proteome of WI N. naja venom (NnV) was deciphered by high resolution mass spectrometry analysis of venom, further fractionated by gel filtration (GF) or RP-HPLC followed by SDS-PAGE and then tandem mass spectrometric analysis of protein bands. The efficacy of commercial polyantivenom (PAV) towards WINnV was assessed by ELISA, immuno-blot, neutralization, and venom-PAV immunoaffinity chromatography studies. Results: Proteomic analysis of WINnV, GF fractions, and SDS-PAGE protein bands of RP-HPLC and GF peaks identified 14, 34, 40, and 54, distinct proteins, respectively, when searched against Elapidae database. The biochemical properties of WINnV correlated well with its proteome composition and pathophysiology of cobra envenomation, including neuroparalysis. This study also highlighted the differences in proteome composition between WINnV and previously reported Eastern India NnV. The tested antivenoms exhibited poor immuno-recognition and neutralization of low molecular mass proteins (<20 kDa), such as three-finger toxins, the major class of protein in WINnV. Conclusion: Improvements in production protocols of antivenoms is the necessity of the hour, supplemented with antibodies raised against the poorly recognized toxins.
机译:背景:Snakebite是热带国家的严重问题,包括印度次大陆。从印度西部(WI)报道了Cobra Bites的首屈一指的案件。研究设计与方法:通过高分辨率质谱分析,通过凝胶过滤(GF)或RP-HPLC,然后串联质谱分析,通过高分辨率质谱分析来破坏Wi NJA毒液(NNV)的蛋白质组。蛋白质带。通过ELISA,免疫印迹,中和和毒液 - 瓦免疫亲和性色谱研究评估了商业聚糖赛(PAV)向WinNV的疗效。结果:当搜索在针对Elapidae数据库时,RP-HPLC和RP-HPLC和GF峰的蛋白质组学分析分别鉴定了14,34,40和54个,不同的蛋白质。 WinNV的生化特性与其蛋白质组组成和COBRA Envenomation的病理生理学相关,包括神经分析。本研究还强调了WinnV与先前报道的蛋白质组组成的差异。测试的抗静电子表现出差的免疫识别和中和低分子量蛋白(<20kDa),例如三指毒素,WinNV中的主要类蛋白质。结论:抗静电子的生产方案的改进是当时的必要性,补充有针对令人难以置信的毒素的抗体。

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