GIANLUCA, Cioci, Alain RIVET, Jaroslav KOCA and Serge PEREZ. Conformational Analysis of Complex Oligosaccharides: The CICADA Approach to the Uromodulin O-Glycans. Carbohydrate Research. 2004, vol. 339, No 4, p. 949-959. ISSN 0008-6215.
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Basic information
Original name Conformational Analysis of Complex Oligosaccharides: The CICADA Approach to the Uromodulin O-Glycans
Name in Czech Konformační analýza složitých oligosacharidů
Authors GIANLUCA, Cioci (250 France), Alain RIVET (250 France), Jaroslav KOCA (203 Czech Republic, guarantor) and Serge PEREZ (250 France).
Edition Carbohydrate Research, 2004, 0008-6215.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10610 Biophysics
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.451
RIV identification code RIV/00216224:14310/04:00010477
Organization unit Faculty of Science
UT WoS 000220389100005
Keywords in English conformational analysis; oligosaccharide; CICADA
Tags CICADA, conformational analysis, oligosaccharide
Changed by Changed by: prof. RNDr. Jaroslav Koča, DrSc., učo 610. Changed: 13/2/2005 16:42.
Abstract
Uromodulin is the pregancy associated Tamm-Horsfall glycoprotein, with ability to inhibit T-cell proliferation. Pregnancy-associated structural changes mainly occur in the O-glycosylation of this glycoprotein. These include up to 12 glycan structures, made up of an unusual core type 2 sequence terminated with one, two, or three sialyl Lewisx sequences; they could serve as E- and P-selectin ligands. The present work focuses on the most complex one; a tetradecamer made up of a type 2 core carrying three sialyl Lewisx branches. Five monosaccharides are assembled by fourteen glycosidic linkages. The conformational behaviour of the constituting disaccharide segments was evaluated using the flexible residue procedure of the MM3 molecular mechanics procedure. For each disaccharide, the adiabatic energy surface, along with the local energy minima have been established. All these results were used for the generation, prior to complete optimization of the tetradecamer. This was followed by a complete exploration of conformational hyperspace throughout the use of Single Coordinate Method as implemented in the CICADA program. Despite the potential flexibility of the tetradecasaccharide, only four conformational families occur, accounting for more than 95% of the total low energy conformations. For each family, the molecular properties (electrostatic, lipophilicity and hydrogen potential) have been studied. The shape of the tetradecasaccharide is best described as a flat ribbon, flanked by three branches having terminal sialyl residues. Two of the branches interact through non-bonded interactions, bringing further energy stabilization, and limiting the conformational flexibility of the sialyl residues. Only one branch maintains the original conformational features of sialyl Lewisx. The O-glycan can be seen as a fascinating example of dendrimeric structure, where the spatial arrangement of three S-Lex epitopes throughout their complementary presentations for interactions with E- and P-selectins.
Abstract (in Czech)
Konformační analýza složitých oligosacharidů
Links
MSM 143100005, plan (intention)Name: Strukturně-funkční vztahy biomolekul a jejich role v metabolismu
Investor: Ministry of Education, Youth and Sports of the CR, Biomolecular Structure-function Relationships and their role in the Metabolism
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