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Göteborgs universitets publikationer

Computational studies on the interaction of ABO-active saccharides with the norovirus VA387 capsid protein can explain experimental binding data

Författare och institution:
Chaitanya A. K. Koppisetty (Institutionen för data- och informationsteknik, Datavetenskap, Bioinformatik (Chalmers), Chalmers); Waqas Nasir (Institutionen för data- och informationsteknik, Datavetenskap, Bioinformatik (Chalmers), Chalmers); F. Strino (-); Gustaf E Rydell (Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin); Göran Larson (Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin); Per-Georg Nyholm (Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi)
Publicerad i:
Journal of Computer-Aided Molecular Design, 24 ( 5 ) s. 423-431
ISSN:
0920-654X
Publikationstyp:
Artikel, refereegranskad vetenskaplig
Publiceringsår:
2010
Språk:
engelska
Fulltextlänk:
Sammanfattning (abstract):
Norovirus strains are known to cause recurring epidemics of winter vomiting disease. The crystal structure of the capsid protein of VA387, a representative of the clinically important GII.4 genocluster, was recently solved in complex with histo-blood group A- and B-trisaccharides. However, the VA387 strain is known to bind also to other natural carbohydrates for which detailed structural information of the complexes is not available. In this study we have computationally explored the fit of the VA387 with a set of naturally occurring carbohydrate ligands containing a terminal alpha 1,2-linked fucose. MD simulations both with explicit and implicit solvent models indicate that type 1 and 3 extensions of the ABO-determinant including ALe(b) and BLe(b) pentasaccharides can be well accommodated in the site. Scoring with Glide XP indicates that the downstream extensions of the ABO-determinants give an increase in binding strength, although the alpha 1,2-linked fucose is the single strongest interacting residue. An error was discovered in the geometry of the GalNAc-Gal moiety of the published crystal structure of the A-trisaccharide/VA387 complex. The present modeling of the complexes with histo-blood group A-active structures shows some contacts which provide insight into mutational data, explaining the involvement of I389 and Q331. Our results can be applicable in structure-based design of adhesion inhibitors of noroviruses.
Ämne (baseras på Högskoleverkets indelning av forskningsämnen):
NATURVETENSKAP ->
Biologiska vetenskaper ->
Strukturbiologi
TEKNIK OCH TEKNOLOGIER ->
Industriell bioteknik
MEDICIN OCH HÄLSOVETENSKAP ->
Klinisk medicin ->
Annan klinisk medicin ->
Klinisk kemi
MEDICIN OCH HÄLSOVETENSKAP ->
Medicinsk bioteknologi ->
Medicinsk bioteknologi (med inriktning mot cellbiologi)
Nyckelord:
Norovirus, Blood group determinants, ABO-saccharides, Molecular, docking, Molecular dynamics, blood group antigens, norwalk virus-infection, nonsense mutation, structural basis, gii-4 norovirus, secretor fut2, resistance, recognition, phenotype
Postens nummer:
123371
Posten skapad:
2010-06-24 11:36
Posten ändrad:
2016-06-28 15:39

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