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Lipolytic activity of ricin from Ricinus sanguineus and Ricinus communis on neutral lipids.

机译:蓖麻和蓖麻蓖麻毒蛋白蓖麻脂对中性脂质的脂解活性。

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摘要

The present study was carried out with a view of determining ricin lipolytic activity on neutral lipids in emulsion and in a membrane-like model. Using 2,3-dimercapto-1-propanol tributyrate (BAL-TC(4)) as substrate, the lipolytic activity of ricin was found to be proportional to ricin and substrate concentrations, with an apparent K(m) (K(m,app)) of 2.4 mM, a k(cat) of 200 min(-1) and a specific activity of 1.0 unit/mg of protein. This work was extended to p-nitrophenyl (pNP) fatty acid esters containing two to twelve carbon atoms. Maximum lipolytic activity was registered on pNP decanoate (pNPC(10)), with a K(m,app) of 3.5 mM, a k(cat) of 173 min(-1) and a specific activity of 3.5 units/mg of protein. Ricin lipolytic activity is pH and galactose dependent, with a maximum at pH 7.0 in the presence of 0.2 M galactose. Using the monolayer technique with dicaprin as substrate, ricin showed a lipolytic activity proportional to the ricin concentration at 20 mN/m, which is dependent on the surface pressure of the lipid monolayer and is detectable up to 30 mN/m, a surface pressure that is of the same order of magnitude as that of natural cell membranes. The methods based on pNPC(10) and BAL-TC(4) hydrolysis are simple and reproducible; thus they can be used for routine studies of ricin lipolytic activity. Ricin from Ricinus communis and R. sanguineus were treated with diethyl p-nitrophenylphosphate, an irreversible serine esterase inhibitor, and their lipolytic activities on BAL-TC(4) and pNPC(10), and cytotoxic activity, were concurrently recorded. A reduction in lipolytic activity was accompanied by a decrease in cytotoxicity on Caco2 cells. These data support the idea that the lipolytic activity associated with ricin is relevant to a lipase whose activity is pH and galactose dependent, sensitive to diethyl p-nitrophenylphosphate, and that a lipolytic step may be involved in the process of cell poisoning by ricin. Both colorimetric tests used in this study are sensitive enough to be helpful in the detection of possible lipolytic activities associated with other cytotoxins or lectins.
机译:进行本研究的目的是确定蓖麻毒蛋白对乳状液和膜状模型中性脂质的脂解活性。使用2,3-二巯基-1-丙醇三丁酸酯(BAL-TC(4))作为底物,蓖麻毒素的脂解活性与蓖麻毒素和底物浓度成正比,表观K(m)(K(m, app)),2.4 mM,ak(cat)为200 min(-1)和1.0单位/ mg蛋白质的比活。这项工作扩展到了包含2至12个碳原子的对硝基苯基(pNP)脂肪酸酯。最大脂解活性在pNP癸酸酯(pNPC(10))上记录,K(m,app)为3.5 mM,k(cat)为173 min(-1),比活性为3.5单位/ mg蛋白质。蓖麻毒素的脂解活性是pH和半乳糖依赖性的,在0.2M半乳糖的存在下在pH 7.0下最大。使用以双caprin为底物的单层技术,蓖麻毒素在20 mN / m时显示出与蓖麻毒素浓度成比例的脂解活性,这取决于脂质单层的表面压力,最高可检测到30 mN / m的表面压力。与天然细胞膜的数量级相同。基于pNPC(10)和BAL-TC(4)水解的方法简单且可重现。因此,它们可用于蓖麻毒素脂解活性的常规研究。用不可逆的丝氨酸酯酶抑制剂二硝基对硝基苯基磷酸二乙酯处理来自蓖麻和蓖麻的蓖麻毒素,并同时记录它们对BAL-TC(4)和pNPC(10)的脂解活性和细胞毒性。脂解活性的降低伴随着对Caco2细胞的细胞毒性的降低。这些数据支持这样的想法,即与蓖麻毒蛋白相关的脂解活性与脂酶有关,该酶的活性是pH和半乳糖依赖性的,对二硝基对硝基苯基磷酸二酯敏感,并且脂解步骤可能参与了蓖麻毒蛋白对细胞的毒性过程。本研究中使用的两种比色法都足够灵敏,有助于检测与其他细胞毒素或凝集素相关的可能的脂解活性。

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