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用偏高碘酸盐-氰基硼氢化物混合物对蓖麻毒素中的碳水化合物进行修饰。对毒性和体内分布的影响。

Modification of the carbohydrate in ricin with metaperiodate-cyanoborohydride mixtures. Effects on toxicity and in vivo distribution.

作者信息

Thorpe P E, Detre S I, Foxwell B M, Brown A N, Skilleter D N, Wilson G, Forrester J A, Stirpe F

出版信息

Eur J Biochem. 1985 Feb 15;147(1):197-206. doi: 10.1111/j.1432-1033.1985.tb08737.x.

Abstract

Attempts to target antibody-ricin conjugates (immunotoxins) to designated cell types in vivo may be thwarted by their rapid clearance by hepatic reticuloendothelial cells which have receptors that recognise oligosaccharide side chains on the toxin. The B-chain of ricin contains high mannose type oligosaccharides and the A-chain contains a complex unit (GlcNAc)2-Fuc-Xyl-(Man)4-6, all of which potentially could be recognised by the reticuloendothelial system. Treatment of ricin with a mixture of sodium metaperiodate and sodium cyanoborohydride at pH 3.5 resulted in oxidative cleavage of the carbohydrates and reduction of the aldehyde groups thus formed to primary alcohols. By conducting the modification procedure at acidic pH, both the possibility of Schiff's base formation between the aldehyde groups and amino groups in the protein and the possibility of non-specific oxidation of amino acids were minimised. The extent of the carbohydrate modification depended on the duration of treatment, resulting maximally in the destruction of 13 of the 18 mannose residues and of all xylose and fucose. The toxicity of the modified toxin to cells in culture declined by up to 90% as the carbohydrate was destroyed. This was not due to a reduced ability of the B-chain to bind to cells or of the A-chain to inactivate ribosomes. In contrast to the in vitro results, the toxicity of the modified toxin to mice and rats was elevated by up to fourfold. The modification greatly reduced the clearance of the toxin by non-parenchymal cells in the liver and prevented the damage to hepatic Kupffer and sinusoidal cells and to the red pulp of the spleen that is inflicted by the native toxin. The elevated toxicity to animals appears to be because the modified toxin evades the reticuloendothelial system and persists in the bloodstream for longer periods, thus resulting in lethal damage to vital tissues in the animal at lower dosage. The results suggest that immunotoxins prepared from modified ricin would not be readily cleared by the reticuloendothelial system and so be more effective at killing their target cells.

摘要

在体内将抗体 - 蓖麻毒素偶联物(免疫毒素)靶向特定细胞类型的尝试可能会受到阻碍,因为肝网状内皮细胞具有识别毒素上寡糖侧链的受体,会使其迅速清除。蓖麻毒素的B链含有高甘露糖型寡糖,A链含有一个复合单元(GlcNAc)2 - Fuc - Xyl -(Man)4 - 6,所有这些都有可能被网状内皮系统识别。在pH 3.5条件下,用偏高碘酸钠和氰基硼氢化钠的混合物处理蓖麻毒素,导致碳水化合物发生氧化裂解,并将由此形成的醛基还原为伯醇。通过在酸性pH下进行修饰过程,可将醛基与蛋白质中的氨基之间形成席夫碱的可能性以及氨基酸非特异性氧化的可能性降至最低。碳水化合物修饰的程度取决于处理时间,最多可导致18个甘露糖残基中的13个以及所有木糖和岩藻糖被破坏。随着碳水化合物被破坏,修饰后的毒素对培养细胞的毒性下降了高达90%。这并非由于B链与细胞结合的能力降低或A链使核糖体失活的能力降低。与体外结果相反,修饰后的毒素对小鼠和大鼠的毒性提高了高达四倍。这种修饰大大降低了肝脏非实质细胞对毒素的清除,并防止了天然毒素对肝库普弗细胞、窦状细胞以及脾脏红髓造成的损伤。对动物毒性升高似乎是因为修饰后的毒素避开了网状内皮系统,并在血液中持续更长时间,从而在较低剂量下对动物的重要组织造成致命损伤。结果表明,由修饰后的蓖麻毒素制备的免疫毒素不易被网状内皮系统清除,因此在杀死靶细胞方面更有效。

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