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Isolation and biological characterization of a basic phospholipase A_2 from Bothrops jararacussu snake venom

机译:蛇毒(Bothrops jararacussu)蛇毒中碱性磷脂酶A_2的分离及生物学特性

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A phospholipase A_2 has been isolated from Bothrops jararacussu venom from snakes that inhabit the northeast region of Argentina. The present study describes in vivo and in vitro biological activities of phospholipase A_2 from B. jararacussu as well as isolation details of its. Venom was obtained by milking of adult snakes which were housing in wood reptile cages of varying dimensions in heated (20-30℃) rooms. Snakes received a weekly diet of mice and water was available ad libitum for drinking and soaking. The enzyme was purified by gel filtration on a Sephadex G-75 column followed by ion exchange chromatography on a SP-Sephadex C25 column. The major peak belonging to proteins was retained in the cation exchanger and then eluted using a concentration gradient of KCl that exhibited phospholipase activity. This basic PLA_2 consists of a single polypeptide chain with a molecular mass of 15.6 kDa. It had a high indirect hemolytic activity and produced a significant paw edema reaction in mice. The enzyme showed a low lethality (LD_(50) 148.6 μg) when was administered i.p. but exhibited elevated myotoxic effects in vivo by increasing plasma CK activity of injected mice, corroborated results by the histological observations of samples of gastrocnemius muscle. Myonecrosis is the result of intense destruction of muscular fibers that involves local infiltration of inflammatory cells and leads to the highest peak of CK level just after 1 hour mice injection. Moreover, the isolated enzyme showed anticoagulant activity, evaluated on sheep platelet-poor plasma which recalcification time was prolonged after incubation with the isolated phospholipase A_2. These findings showed that this phospholipase, isolated by only two simple chromatographic steps, possesses high edematogenic and myotoxic activities. However, despite the low lethal activity, this enzyme would contribute markedly to the pathophysiology of the bothropic envenomation.
机译:从阿根廷东北部的蛇类中的Bothrops jararacussu毒液中分离出了磷脂酶A_2。本研究描述了来自jararacussu的磷脂酶A_2的体内和体外生物学活性及其分离细节。毒液是通过成年蛇的挤奶获得的,成年蛇被安置在加热(20-30℃)的房间中不同尺寸的木质爬行动物笼中。蛇每周接受一次小鼠饮食,可随意饮用水以供饮用和浸泡。通过在Sephadex G-75柱上进行凝胶过滤,然后在SP-Sephadex C25柱上进行离子交换色谱法,纯化酶。属于蛋白质的主峰保留在阳离子交换剂中,然后使用表现出磷脂酶活性的KCl浓度梯度洗脱。这个基本的PLA_2由一条分子量为15.6 kDa的多肽链组成。它具有很高的间接溶血活性,并在小鼠中产生了明显的爪水肿反应。腹膜内给药后,该酶显示出低致死率(LD_(50)148.6μg)。但通过增加注射小鼠的血浆CK活性在体内表现出升高的肌毒性作用,通过腓肠肌样本的组织学观察证实了这一结果。肌坏死是肌肉纤维强烈破坏的结果,其中涉及炎性细胞的局部浸润,并在刚注射1小时后导致CK水平的最高峰。而且,分离的酶显示出抗凝活性,在贫血小板的绵羊血浆上评估,与分离的磷脂酶A_2一起孵育后重钙化时间延长。这些发现表明,仅通过两个简单的色谱步骤即可分离出的这种磷脂酶具有很高的产生水肿和肌肉毒性的活性。然而,尽管致死活性低,但这种酶仍将显着促进双性毒物的病理生理。

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