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多烯抗生素鲁西诺霉素引起溶血的化学计量学

Stoichiometry of hemolysis by the polyene antibiotic lucensomycin.

作者信息

Strom R, Crifò C, Eusebi F, Sabetta F, Oratore A

出版信息

Biochim Biophys Acta. 1976 Dec 14;455(3):961-72. doi: 10.1016/0005-2736(76)90064-x.

Abstract

The stoichiometry of hemolysis by the polyene antibiotic lucensomycin was investigated. It appears that hemolysis occurs only when a relatively high fraction (probably between 15 and 40%) of the cholesterol sites in the erythrocyte membrane have combined with the polyene. Also in phospholipid-cholesterol vesicles the increase of permeability requires occupancy of 40-50% of the existing cholesterol sites. As for the possible cooperative effect in the hemolytic process, it is probable that several (at least 9-10) lucensomycin-cholesterol adducts must interact on each side of the membrane to form an aqueous channel; the distribution of these adducts in the erythrocyte membrane occurs, however, apparently at random.

摘要

对多烯抗生素鲁西诺霉素的溶血化学计量学进行了研究。似乎只有当红细胞膜中相当一部分(可能在15%至40%之间)的胆固醇位点与多烯结合时才会发生溶血。在磷脂 - 胆固醇囊泡中,通透性的增加也需要占据现有胆固醇位点的40 - 50%。至于溶血过程中可能的协同作用,很可能在膜的每一侧有几个(至少9 - 10个)鲁西诺霉素 - 胆固醇加合物相互作用以形成一个水通道;然而,这些加合物在红细胞膜中的分布显然是随机的。

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