Garidel Patrick, Kaconis Yani, Heinbockel Lena, Wulf Matthias, Gerber Sven, Munk Ariane, Vill Volkmar, Brandenburg Klaus
Physikalische Chemie, Martin-Luther-Universität Halle/Wittenberg, Mühlpforte 1, D-06108 Halle/Saale, Germany.
Forschungszentrum Borstel, Leibniz-Zentrum für Medizin und Biowissenschaften, Parkallee 1-40, D-23845 Borstel, Germany.
Open Biochem J. 2015 Aug 31;9:49-72. doi: 10.2174/1874091X01509010049. eCollection 2015.
Glycolipids are amphiphilic molecules which bear an oligo- or polysaccharide as hydrophilic head group and hydrocarbon chains in varying numbers and lengths as hydrophobic part. They play an important role in life science as well as in material science. Their biological and physiological functions are quite diverse, ranging from mediators of cell-cell recognition processes, constituents of membrane domains or as membrane-forming units. Glycolipids form an exceptional class of liquid-crystal mesophases due to the fact that their self-organisation obeys more complex rules as compared to classical monophilic liquid-crystals. Like other amphiphiles, the supra-molecular structures formed by glycolipids are driven by their chemical structure; however, the details of this process are still hardly understood. Based on the synthesis of specific glycolipids with a clearly defined chemical structure, e.g., type and length of the sugar head group, acyl chain linkage, substitution pattern, hydrocarbon chain lengths and saturation, combined with a profound physico-chemical characterisation of the formed mesophases, the principles of the organisation in different aggregate structures of the glycolipids can be obtained. The importance of the observed and formed phases and their properties are discussed with respect to their biological and physiological relevance. The presented data describe briefly the strategies used for the synthesis of the used glycolipids. The main focus, however, lies on the thermotropic as well as lyotropic characterisation of the self-organised structures and formed phases based on physico-chemical and biophysical methods linked to their potential biological implications and relevance.
糖脂是两亲性分子,其具有寡糖或多糖作为亲水头基,以及数量和长度各异的烃链作为疏水部分。它们在生命科学以及材料科学中发挥着重要作用。其生物学和生理学功能多种多样,包括细胞间识别过程的介质、膜结构域的组成成分或作为膜形成单元。糖脂形成了一类特殊的液晶中间相,因为与经典的单亲性液晶相比,它们的自组装遵循更复杂的规则。与其他两亲分子一样,糖脂形成的超分子结构由其化学结构驱动;然而,这一过程的细节仍知之甚少。基于合成具有明确化学结构的特定糖脂,例如糖头基的类型和长度、酰基链连接、取代模式、烃链长度和饱和度,并结合对形成的中间相进行深入的物理化学表征,可以获得糖脂在不同聚集结构中的组装原理。根据所观察到的相及其性质与生物学和生理学相关性,讨论了它们的重要性。所呈现的数据简要描述了用于合成所用糖脂的策略。然而,主要重点在于基于与它们潜在的生物学意义和相关性相关的物理化学和生物物理方法,对自组装结构和形成相的热致和溶致表征。