Organization of gangliosides into membrane nanodomains

被引:18
|
作者
Sarmento, Maria J. [1 ]
Ricardo, Joana C. [1 ]
Amaro, Mariana [1 ]
Sachl, Radek [1 ]
机构
[1] Czech Acad Sci, J Heyrovsky Inst Phys Chem, Dolejskova 3, Prague 18223 8, Czech Republic
关键词
AFM; diffusion; diffusion laws; gangliosides; GM(1); lipid bilayers; MC-FRET; membrane model systems; nanodomains; phase separation; ATOMIC-FORCE MICROSCOPY; SUPPORTED LIPID-BILAYERS; GIANT UNILAMELLAR VESICLES; LATERAL PHASE-SEPARATION; CHAIN BASE COMPOSITION; SIALIC-ACID RESIDUES; GM1; GANGLIOSIDE; PLASMA-MEMBRANE; DOMAIN FORMATION; ALPHA-HYDROXYLATION;
D O I
10.1002/1873-3468.13871
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gangliosides are glycosphingolipids consisting of a ceramide base and a bulky sugar chain that contains one or more sialic acids. This unique structure endows gangliosides with a strong tendency to self-aggregate in solution, as well as in cellular membranes, where they can form nanoscopic assemblies called ganglioside nanodomains. As gangliosides are important biological molecules involved in a number of physiological processes, characterization of their lateral organization in membranes is essential. This review aims at providing comprehensive information about the nanoscale organization of gangliosides in various synthetic models. To this end, the impact of the hydrophobic backbone and the headgroup on the segregation of gangliosides into nanodomains are discussed in detail, as well as the way in which the properties of nanodomains are affected by ligand binding. Small size makes the characterization of ganglioside nanodomains challenging, and we thus highlight the biophysical methods that have advanced this research, such as Monte Carlo Forster resonance energy transfer, atomic force microscopy and approaches based on molecular diffusion.
引用
收藏
页码:3668 / 3697
页数:30
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