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1.
J Struct Biol ; 209(1): 107407, 2020 01 01.
Article in English | MEDLINE | ID: mdl-31698075

ABSTRACT

Although the 3D structure of carbohydrates is known to contribute to their biological roles, conformational studies of sugars are challenging because their chains are flexible in solution and consequently the number of 3D structural restraints is limited. Here, we investigate the conformational properties of the tetrasaccharide building block of the Lytechinus variegatus sulfated fucan composed of the following structure [l-Fucp4(SO3-)-α(1-3)-l-Fucp2,4(SO3-)-α(1-3)-l-Fucp2(SO3-)-α(1-3)-l-Fucp2(SO3-)] and the composing monosaccharide unit Fucp, primarily by nuclear magnetic resonance (NMR) experiments performed at very low temperatures and using H2O as the solvent for the sugars rather than using the conventional deuterium oxide. By slowing down the fast chemical exchange rates and forcing the protonation of labile sites, we increased the number of through-space 1H-1H distances that could be measured by NMR spectroscopy. Following this strategy, additional conformational details of the tetrasaccharide and l-Fucp in solution were obtained. Computational molecular dynamics was performed to complement and validate the NMR-based measurements. A model of the NMR-restrained 3D structure is offered for the tetrasaccharide.


Subject(s)
Fucose/chemistry , Molecular Conformation , Oligosaccharides/ultrastructure , Polysaccharides/ultrastructure , Animals , Carbohydrates/chemistry , Lytechinus/chemistry , Magnetic Resonance Spectroscopy , Molecular Dynamics Simulation , Oligosaccharides/chemistry , Polysaccharides/chemistry
2.
J Biol Chem ; 291(18): 9425-37, 2016 Apr 29.
Article in English | MEDLINE | ID: mdl-26917726

ABSTRACT

Early metazoans had to evolve the first cell adhesion mechanism addressed to maintain a distinctive multicellular morphology. As the oldest extant animals, sponges are good candidates for possessing remnants of the molecules responsible for this crucial evolutionary innovation. Cell adhesion in sponges is mediated by the calcium-dependent multivalent self-interactions of sulfated polysaccharides components of extracellular membrane-bound proteoglycans, namely aggregation factors. Here, we used atomic force microscopy to demonstrate that the aggregation factor of the sponge Desmapsamma anchorata has a circular supramolecular structure and that it thus belongs to the spongican family. Its sulfated polysaccharide units, which were characterized via nuclear magnetic resonance analysis, consist preponderantly of a central backbone composed of 3-α-Glc1 units partially sulfated at 2- and 4-positions and branches of Pyr(4,6)α-Gal1→3-α-Fuc2(SO3)1→3-α-Glc4(SO3)1→3-α-Glc→4-linked to the central α-Glc units. Single-molecule force measurements of self-binding forces of this sulfated polysaccharide and their chemically desulfated and carboxyl-reduced derivatives revealed that the sulfate epitopes and extracellular calcium are essential for providing the strength and stability necessary to sustain cell adhesion in sponges. We further discuss these findings within the framework of the role of molecular structures in the early evolution of metazoans.


Subject(s)
Biological Evolution , Calcium/chemistry , Polysaccharides/chemistry , Porifera/chemistry , Sulfates/chemistry , Animals , Calcium/metabolism , Microscopy, Atomic Force , Polysaccharides/metabolism , Polysaccharides/ultrastructure , Porifera/metabolism , Porifera/ultrastructure , Sulfates/metabolism
3.
J Struct Biol ; 145(3): 216-25, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14960372

ABSTRACT

We have studied the ultrastructure of acidic polysaccharides from the cell walls of brown algae using a variety of electron microscopy techniques. Polysaccharides from Padina gymnospora present self assembled structures, forming trabecular patterns. Purified fractions constituted by alginic acid and sulfated fucan also form well-organized ultrastructures, but the pattern of organization varies depending on the polysaccharide species. Alginic acid presents sponge-like structures. Sulfated fucan exhibits particles with polygonal forms with a polycrystalline structure. These particles are in fact constituted by sulfated fucan molecules since they are recognized by a lectin specific for alpha-l-fucosyl residues. X-ray microanalysis reveal that S is a constituent element, as expected for sulfated groups. Finally, an exhaustive purified sulfated fucan shows the same ultrastructure formed by polygonal forms. Furthermore, elemental analyses of acidic polysaccharides indicate that they retain Zn, when algae were collected from a contaminated area. This observation is supported by direct quantification of heavy metal in the biomass and also in the solubilized polysaccharides compared with the algae from a non-contaminated site. We conclude that these molecules have specific ultrastructure and elemental composition; and act as metal binder for the nucleation and precipitation of heavy metals when the algae are exposed to a metal contaminated environment.


Subject(s)
Phaeophyceae/ultrastructure , Polysaccharides/ultrastructure , Alginates/chemistry , Cadmium/chemistry , Cell Wall/ultrastructure , Chromatography, Ion Exchange , Crystallography, X-Ray , Fucose/chemistry , Glucuronic Acid/chemistry , Gold Colloid/chemistry , Hexuronic Acids/chemistry , Lectins/chemistry , Microscopy, Electron , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Polysaccharides/chemistry , Protein Conformation , Sulfur/chemistry , Zinc/chemistry
4.
Appl Biochem Biotechnol ; 59(2): 135-43, 1996 May.
Article in English | MEDLINE | ID: mdl-8678483

ABSTRACT

Different strains of baker's yeast (Saccharomyces cerevisiae) were imaged with an atomic force microscope (AFM). The images of uncoated and nonfixed samples were reproducible with high-constrast and nanometer-resolution. Molecules from the polysaccharide surface of the cell wall were pictured and the distance of atoms was measured. The preparation of samples was easy, suggesting that AFM is a useful tool in this type of analyses.


Subject(s)
Biotransformation , Saccharomyces cerevisiae/metabolism , Cell Wall/metabolism , Cell Wall/ultrastructure , Microscopy, Atomic Force , Polysaccharides/metabolism , Polysaccharides/ultrastructure , Reproducibility of Results , Saccharomyces cerevisiae/cytology , Saccharomyces cerevisiae/ultrastructure
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