Kocsis Béla, Makszin Lilla, Kilár Anikó, Péterfi Zoltán, Kilár Ferenc
Institute of Medical Microbiology and Immunology, Faculty of Medicine, University of Pécs, Pécs, Hungary.
Institute of Bioanalysis, Faculty of Medicine, University of Pécs, Pécs, Hungary.
Methods Mol Biol. 2017;1600:151-165. doi: 10.1007/978-1-4939-6958-6_15.
Endotoxins (lipopolysaccharides, LPS; lipooligosaccharides, LOS) are components of the envelope of Gram-negative bacteria. These molecules, responsible for both advantageous and harmful biological activity of these microorganisms, are highly immunogenic and directly involved in numerous bacterial diseases in humans, such as Gram-negative sepsis. The characterization of endotoxins is of importance, since their physiological and pathophysiological effects depend on their chemical structure. The differences among the LPS from different bacterial serotypes and their mutants include variations mainly within the composition and length or missing of their O-polysaccharide chains. Microchip electrophoretic methodology enables the structural characterization of LPS molecules from several bacteria and the quantitative evaluation of components of endotoxin extracts. The improved microchip electrophoretic method is based on the direct labeling of endotoxins by covalent binding of a fluorescent dye. The classification of the S-type LPSs can be done according to their electrophoretic profiles, which are characteristics of the respective bacterial strains. According to the number, distribution, and the relative amounts of components in an endotoxin extract, it is possible to differentiate between the S-type endotoxins from different Gram-negative bacterial strains. The microchip electrophoresis affords high-resolution separation of pure and partially purified (e.g., obtained from whole-cell lysate) S and R endotoxins. This microchip technique provides a new, standardizable, fast, and sensitive method for the detection of endotoxins and for the quantitative evaluation of components of an endotoxin extract.
内毒素(脂多糖,LPS;脂寡糖,LOS)是革兰氏阴性菌包膜的组成成分。这些分子既具有这些微生物的有益生物活性,也具有有害生物活性,具有高度免疫原性,直接参与人类的多种细菌性疾病,如革兰氏阴性菌败血症。内毒素的特性很重要,因为它们的生理和病理生理效应取决于其化学结构。不同细菌血清型及其突变体的脂多糖之间的差异主要包括其O-多糖链的组成、长度变化或缺失。微芯片电泳方法能够对内毒素分子进行结构表征,并对内毒素提取物的成分进行定量评估。改进后的微芯片电泳方法基于通过荧光染料的共价结合对内毒素进行直接标记。S型脂多糖可以根据其电泳图谱进行分类,这些图谱是各自细菌菌株的特征。根据内毒素提取物中成分的数量、分布和相对含量,可以区分来自不同革兰氏阴性细菌菌株的S型内毒素。微芯片电泳能够对纯的和部分纯化的(例如,从全细胞裂解物中获得的)S型和R型内毒素进行高分辨率分离。这种微芯片技术为内毒素的检测和内毒素提取物成分的定量评估提供了一种新的、标准化的、快速且灵敏的方法。