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糖脂受体功能的脂质调节。天然和合成糖脂中用于维罗毒素结合的Gal(α1-4)Gal二糖的可及性。

Lipid modulation of glycolipid receptor function. Availability of Gal(alpha 1-4)Gal disaccharide for verotoxin binding in natural and synthetic glycolipids.

作者信息

Boyd B, Magnusson G, Zhiuyan Z, Lingwood C A

机构信息

Department of Microbiology, Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

Eur J Biochem. 1994 Aug 1;223(3):873-8. doi: 10.1111/j.1432-1033.1994.tb19064.x.

Abstract

Verotoxins bind to glycosphingolipids containing terminal Gal(alpha 1-4)Gal residues. Globotriaosylceramide is the most effective receptor for verotoxin-1 in vitro and is the functional plasma-membrane receptor which mediates cytopathology for most sensitive cells. Binding of verotoxin-1 to a series of galabiose-containing or globotriaose-containing synthetic glycolipids with monoalkylsulfides and bisalkylsulfides or sulfones as the lipid moiety, have been studied for toxin binding by TLC overlay and in solid phase in the presence of auxiliary lipids. The results demonstrate that for an identical carbohydrate, binding is dramatically altered according to the nature of the lipid moiety. The close proximity of the galabiose sequence and the hydrophobic species also compromised recognition. The lipid environment is also a major determinant of receptor function, since species that were effective, even preferred toxin receptors as monitored by TLC overlay, were not necessarily recognized in the presence of auxiliary lipids. Certain glycolipids, which were not recognized by TLC overlay, were nevertheless found to be effective receptors in an auxiliary lipid matrix. These results demonstrate the crucial role of the lipid moiety in verotoxin/glycolipid recognition and are discussed in relation to toxin pathogenesis and glycolipid receptor function.

摘要

维罗毒素与含有末端Gal(α1-4)Gal残基的糖鞘脂结合。体外实验中,球三糖神经酰胺是维罗毒素-1最有效的受体,也是介导大多数敏感细胞发生细胞病变的功能性质膜受体。通过薄层层析覆盖法和在辅助脂质存在下的固相法,研究了维罗毒素-1与一系列含有半乳糖二糖或球三糖的合成糖脂(其脂质部分为单烷基硫化物、双烷基硫化物或砜)的结合情况,以检测毒素结合。结果表明,对于相同的碳水化合物,根据脂质部分的性质,结合情况会发生显著变化。半乳糖二糖序列与疏水基团的紧密接近也会影响识别。脂质环境也是受体功能的主要决定因素,因为通过薄层层析覆盖法监测到的有效甚至是首选毒素受体的物质,在辅助脂质存在时不一定能被识别。某些未被薄层层析覆盖法识别的糖脂,在辅助脂质基质中却被发现是有效的受体。这些结果证明了脂质部分在维罗毒素/糖脂识别中的关键作用,并结合毒素发病机制和糖脂受体功能进行了讨论。

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