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Stereochemical assignment of diastereomeric imidazolidinone ring containing bicyclic sugar-peptide addects: NMR Spectroscopy and molecular calculations
Stockholm University, Faculty of Science, Department of Organic Chemistry.
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2004 In: European Journal of Organic Chemistry, ISSN 1434-193X, no 22, 4641-4647 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. no 22, 4641-4647 p.
URN: urn:nbn:se:su:diva-23897OAI: diva2:195196
Part of urn:nbn:se:su:diva-538Available from: 2005-05-13 Created: 2005-05-13Bibliographically approved
In thesis
1. Computational Analysis of Carbohydrates: Dynamical Properties and Interactions
Open this publication in new window or tab >>Computational Analysis of Carbohydrates: Dynamical Properties and Interactions
2005 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

In this thesis a computational complement to experimental observables will be presented. Computational tools such as molecular dynamics and quantum chemical tools will be used to aid in the interpretation of experimentally (NMR) obtained structural data. The techniques are applied to study the dynamical features of biologically important carbohydrates and their interaction with proteins. When evaluating conformations, molecular mechanical methods are commonly used. Paper I, highlights some important considerations and focuses on the force field parameters pertaining to carbohydrate moieties. Testing of the new parameters on a trisaccharide showed promising results. In Paper II, a conformational analysis of a part of the repeating unit of a Shigella flexneri bacterium lipopolysaccharide using the modified force field revealed two major conformational states. The results showed good agreement with experimental data. In Paper III, a trisaccharide using Langevin dynamics was investigated. The approach used in the population analysis included a least-square fit technique to match T1 elaxation parameters. The results showed good agreement with experimental T-ROE build-up curves, and three states were concluded to be involved. In Paper IV, carbohydrate moieties were used in the development of prodrug candidates, to “hide” peptide opioid receptor agonists. Langevin dynamics and quantum chemical methods were employed to elucidate the structural preference of the compound. The results showed a chemical shift difference between hydrogens across the ring for the two isomers as well as a difference in the coupling constant, when taking the dynamics into account. In Paper V, the interaction of the Salmonella enteritidis bacteriophage P22 with its host bacterium, involves an initial hydrolysis of the O-antigenic polysaccharide (O-PS). Docking calculations were used to examine the binding between the Phage P22 tail-spike protein and the O-PS repeating unit. Results indicated a possible active site in conjunction with NMR measurements.

Place, publisher, year, edition, pages
Stockholm: Institutionen för organisk kemi, 2005. 208 p.
Carbohydrate, DFT, ab initio, docking calculations, Molecular dynamics, Langevin Dynaimcs, structure analysis, carbohydrate-protein interaction, Chemical shift calculations, Spin spin coupling constants.
National Category
Organic Chemistry
urn:nbn:se:su:diva-538 (URN)91-7155-080-1 (ISBN)
Public defence
2005-06-03, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 12 A, Stockholm, 10:00 (English)
Available from: 2005-05-13 Created: 2005-05-13 Last updated: 2010-02-03Bibliographically approved

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