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Leucurogin, a new recombinant disintegrin cloned from Bothrops leucurus (white-tailed-jararaca) with potent activity upon platelet aggregation and tumor growth

机译:Leucurogin,一种从Bothrops leucurus(white-tailed-jararaca)克隆的新型重组解整合素,对血小板聚集和肿瘤生长具有有效活性

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摘要

Disintegrins and disintegrins-like proteins are able to inhibit platelet aggregation and integrin-mediated cell adhesion. the aim of this study was to produce one disintegrin-like cloned from Bothrops leucurus venom gland and to characterize it regarding biological activity. the recombinant protein was purified by one step procedure involving anion-exchange chromatography (DEAE-cellulose) and presented a molecular mass of 10.4 kDa. the purified protein was able to inhibit platelet aggregation induced by collagen (IC(50) = 0.65 mu M) and to inhibit growth of Ehrlich tumor implanted in mice by more than 50% after 7 days administration of 10 mu g/day. No effects were observed upon adenosine 5'diphosphate (ADP)-and arachidonic acid (AA)-induced platelet aggregation. the recombinant protein was recognized by an antibody specific for jararhagin one metalloproteinase isolated from Bothrops jararaca venom, and therefore it was named leucurogin. Anti-angiogenesis effect of leucurogin was evaluated by the sponge implant model. After 7 days administration leucurogin inhibited, in a dose dependent way, the vascularization process in the sponge. Leucurogin represents a new biotechnological tool to understand biological processes where disintegrins-like are involved and may help to characterize integrins that can be involved in development and progression of malignant cells. (C) 2011 Elsevier B.V. All rights reserved.
机译:整合素和整合素样蛋白能够抑制血小板聚集和整合素介导的细胞粘附。这项研究的目的是生产一种从Bothrops leucurus蛇毒腺中克隆得到的disintegrin样,并对其生物学活性进行表征。通过涉及阴离子交换色谱法(DEAE-纤维素)的一步法纯化重组蛋白,其分子量为10.4kDa。纯化的蛋白质能够抑制胶原蛋白诱导的血小板凝集(IC(50)= 0.65μM),并且在以10μg /天的剂量给药7天后,能够抑制植入小鼠的Ehrlich肿瘤的生长超过50%。腺苷5'二磷酸(ADP)和花生四烯酸(AA)诱导的血小板聚集没有观察到影响。该重组蛋白被特异于jararhagin的一种金属蛋白蛋白酶的抗体所识别,该金属蛋白酶是从Bothrops jararaca毒液中分离出来的,因此被称为亮氨酸。用海绵植入物模型评估亮氨酸的抗血管生成作用。给药7天后,亮白细胞素以剂量依赖性方式抑制海绵中的血管形成过程。 Leucurogin代表一种新的生物技术工具,可用于理解涉及整合素样物质的生物过程,并可能有助于表征可能参与恶性细胞发育和发展的整联蛋白。 (C)2011 Elsevier B.V.保留所有权利。

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