On the structural significance of the linkage region constituents of N-glycoproteins: an X-ray crystallographic investigation using models and analogs
Autor: | Kuttikode Priya, Duraikkannu Loganathan, Thiruneelakantan Lakshmanan, Desikan Sriram |
---|---|
Rok vydání: | 2003 |
Předmět: |
Models
Molecular Stereochemistry Protein Conformation Biophysics Linkage (mechanical) Crystal structure Crystallography X-Ray Biochemistry law.invention Acetylglucosamine chemistry.chemical_compound Structure-Activity Relationship Protein structure law Amide Moiety Computer Simulation Trisaccharide amide amino acid asparagine bacterial protein carbohydrate derivative galactose glutamine glycoprotein glycoside hydrogen mannose propionamide derivative rhamnose trisaccharide xylose article carbohydrate analysis chemical bond crystal structure Geobacillus stearothermophilus hydrogen bond molecular model priority journal protein assembly protein structure rigidity X ray crystallography Asparagine Binding Sites Carbon Glycolysis Glycoproteins Hydrogen Bonding Protein Binding Protein Subunits Eukaryota Molecular Biology chemistry.chemical_classification Chemistry Hydrogen bond Cell Biology Crystallography Acetamide |
Zdroj: | Biochemical and biophysical research communications. 312(2) |
ISSN: | 0006-291X |
Popis: | The linkage region constituents, namely, 2-acetamido-2-deoxy-beta-D-glucopyranose and asparagine are conserved in the N-glycoproteins of all the eukaryotes. The present work is aimed at understanding the reasons for the occurrence of GlcNAc and Asn as the linkage region constituents. A total of six sugar amides have been designed as models and analogs of the linkage region and their crystal structures have been solved. This is the first report on the X-ray crystallographic investigation of the effect of systematic changes in the linkage sugar as well as its aglycon moiety on the N-glycosidic torsion, psi(N) (O5-C1-N1-C1(')). This also forms the first report on the crystal structure of a model of L-RhabetaAsn, a variant linkage found in the surface layer glycoprotein of Bacillus stearothermophillus. Among the models and analogs examined, the acetamido derivatives of Man and Xyl, the linkage sugars of O-glycoproteins, show a psi(N) value of -114.5 degrees and -121.2 degrees, respectively, deviating maximum from the value of -89.8 degrees reported for the model compound GlcNAcbetaNHAc. The L-Rha and Gal derivatives also show noticeable deviations. The psi(N) values, -89.5 degrees and -91.0 degrees, of the propionamide derivatives of Glc and GlcNAc (analogs of GlcbetaGln and GlcNAcbetaGln, respectively) agree well with those (-93.8 degrees and -89.8 degrees ) reported for their corresponding acetamide derivatives suggesting Gln could serve as well as Asn as the linkage region amino acid. However, the rotational freedom about the additional C-C bond would lead to altered rigidity of the linkage region. An analysis of packing reveals that the molecular assembly of these compounds is driven by different infinite and finite chains of hydrogen bonds. The double pillaring of hydrogen bonds involving the amide groups at C1 and C2 is seen as a unique packing feature characteristic of beta-1-N-acyl derivatives of GlcNAc. Based on the findings of the present study, it is speculated that the linkage region constituents of the eukaryotic N-glycoproteins appear to fulfill three essential structural requirements: rigidity, planarity, and linearity and these are met by the trisaccharide core and Asn at the linkage region. |
Databáze: | OpenAIRE |
Externí odkaz: |