首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Improved method for the isolation, characterization and examination of neuromuscular and toxic properties of selected polypeptide fractions from the crude venom of the Taiwan cobra Naja naja atra.
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Improved method for the isolation, characterization and examination of neuromuscular and toxic properties of selected polypeptide fractions from the crude venom of the Taiwan cobra Naja naja atra.

机译:一种改进的方法,用于从台湾眼镜蛇眼镜蛇眼镜蛇粗蛇毒的粗毒中分离,表征和检查选定的多肽级分的神经肌肉和毒性特性。

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摘要

An improved chromatographic method was developed to isolate and purify polypeptides and proteins from the crude venom of the Taiwan cobra Naja naja atra. The procedure devised is simple, easy to reproduce, and enables large scale isolation of almost all polypeptides and proteins in this cobra venom. Six pure polypeptide fractions of the venom were isolated and characterized using gel filtration on Sephadex G50 (medium), ion exchange chromatography on SP-Sephadex C25, desalting on Sephadex G25 (fine) and preparative HPLC on a RPC 18 column. The neuromuscular activity of these fractions was tested on the chick biventer cervicis nerve-muscle preparation and their toxicity (LD(50)) was determined after i.v. administration in mice. Their antinociceptive activity was tested in the mouse abdominal test by i.v. application. Two of these polypeptide samples had major physiological effects: one acted as a cardiotoxin causing reversible myocardial contractures with no effect on muscle twitches elicited by nerve stimulation (NS); another was a neurotoxin that blocked muscle contractions in response to NS and exogenously added acetylcholine. The cardiotoxic fraction was identified as CTX I, a well-known cardiotoxin present in this venom, and the neurotoxin was identified as neurotoxin-alpha with an LD50 in mice of 0.075[NON-BREAKING SPACE]mg/kg
机译:开发了一种改进的色谱方法,从台湾眼镜蛇眼镜蛇眼镜蛇粗蛇毒的粗毒中分离和纯化多肽和蛋白质。设计的程序简单,易于复制,并能大规模分离该眼镜蛇毒液中的几乎所有多肽和蛋白质。分离并纯化了毒液的六个纯多肽级分,并通过在Sephadex G50(中等)上进行凝胶过滤,在SP-Sephadex C25上进行离子交换色谱,在Sephadex G25上脱盐(精细)和在RPC 18色谱柱上的制备型HPLC进行表征。在鸡biventer宫颈神经肌肉制剂上测试了这些级分的神经肌肉活性,并在静脉内注射后确定了它们的毒性(LD(50))。小鼠给药。它们的抗伤害感受活性通过i.v.应用。这些多肽样品中有两个具有重要的生理作用:一个起心脏毒素的作用,引起可逆的心肌挛缩,对神经刺激(NS)引起的肌肉抽搐没有影响。另一类是神经毒素,它在响应NS和外源添加乙酰胆碱后会阻止肌肉收缩。在该毒液中,心脏毒性部分被鉴定为CTX I,这是一种众所周知的心脏毒素,而神经毒素被鉴定为神经毒素-α,在小鼠中的LD50为0.075 [NON-BREAKING SPACE] mg / kg

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