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鞘脂与富含固醇的有序膜结构域的形成。

Sphingolipids and the formation of sterol-enriched ordered membrane domains.

作者信息

Ramstedt Bodil, Slotte J Peter

机构信息

Department of Biochemistry and Pharmacy, Abo Akademi University, Tykistokatu 6A, 20520 Turku, Finland.

出版信息

Biochim Biophys Acta. 2006 Dec;1758(12):1945-56. doi: 10.1016/j.bbamem.2006.05.020. Epub 2006 Jun 3.

Abstract

This review is focused on the formation of lateral domains in model bilayer membranes, with an emphasis on sphingolipids and their interaction with cholesterol. Sphingolipids in general show a preference for partitioning into ordered domains. One of the roles of cholesterol is apparently to modulate the fluidity of the sphingolipid domains and also to help segregate the domains for functional purposes. Cholesterol shows a preference for sphingomyelin over phosphatidylcholine with corresponding acyl chains. The interaction of cholesterol with different sphingolipids is largely dependent on the molecular properties of the particular sphingolipid in question. Small head group size clearly has a destabilizing effect on sphingolipid/cholesterol interaction, as exemplified by studies with ceramide and ceramide phosphoethanolamine. Ceramides actually displace sterol from ordered domains formed with saturated phosphatidylcholine or sphingomyelin. The N-linked acyl chain is known to be an important stabilizer of the sphingolipid/cholesterol interaction. However, N-acyl phosphatidylethanolamines failed to interact favorably with cholesterol and to form cholesterol-enriched lateral domains in bilayer membranes. Glycosphingolipids also form ordered domains in membranes but do not show a strong preference for interacting with cholesterol. It is clear from the studies reviewed here that small changes in the structure of sphingolipids alter their partitioning between lateral domains substantially.

摘要

本综述聚焦于模型双层膜中侧向结构域的形成,重点关注鞘脂及其与胆固醇的相互作用。一般来说,鞘脂倾向于分配到有序结构域中。胆固醇的作用之一显然是调节鞘脂结构域的流动性,并出于功能目的帮助分离这些结构域。与具有相应酰基链的磷脂酰胆碱相比,胆固醇更倾向于与鞘磷脂结合。胆固醇与不同鞘脂的相互作用在很大程度上取决于所讨论的特定鞘脂的分子特性。小的头部基团尺寸显然对鞘脂/胆固醇相互作用有破坏作用,以神经酰胺和神经酰胺磷酸乙醇胺的研究为例。神经酰胺实际上会将甾醇从由饱和磷脂酰胆碱或鞘磷脂形成的有序结构域中取代出来。已知N-连接的酰基链是鞘脂/胆固醇相互作用的重要稳定剂。然而,N-酰基磷脂酰乙醇胺未能与胆固醇良好相互作用,也未能在双层膜中形成富含胆固醇的侧向结构域。糖鞘脂也会在膜中形成有序结构域,但对与胆固醇相互作用没有强烈偏好。从这里综述的研究可以清楚地看出,鞘脂结构的微小变化会显著改变它们在侧向结构域之间的分配。

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