Dissertation (Metadaten)
Titel:Darstellung photolabiler Mannose-Derivate zur Markierung des Typ-1-fimbrialen Lectins aus E.coli
 
Autor:Mark Walter
 
URN:NBN:urn:nbn:de:gbv:8-diss-9311
 
Fakultät:Mathematisch-Naturwissenschaftliche Fakultät
DDC Sachgebiet:610 Medizin und Gesundheit
 
Datum der mdl. Prüfung:08.12.2003
 
Referent(in):Prof. Dr. Thisbe K. Lindhorst
Korreferent(en) Korreferentin:Prof. Dr. Ulrich Lüning
 
Beschreibung (original):(Keine Zusammenfassung in deutscher Sprache vorhanden.) (No summary in German language.)
 
(übersetzt):Escherichia coli bacteria possess so called type 1 fimbriae to adhere to alpha-mannosyl residues present in the glycocalyx of potential host cells. It has been the goal of this thesis to synthesize mannose derivatives, which are equipped with a photolabile diazirine group to facillitate research, which is aimed at the elucidation of the details of the molecular interaction between the lectin domain FimH and carbohydrates. Eventually, these derivatives could be incubated with FimH and irradiated to allow a peptide digestion and spectrometric investigation of the covalently linked protein-carbohydrate adduct. The diazirine group has been incorporated into the aglycone part of O-glycosides and thiourea-linked derivatives, respectively. To introduce a broad variety of structures a modular concept has been developed using convergent synthesis and the knowledge of graded reactivities of two different isothiocyanato groups in a difunctionalized mannose derivative. In combination with glycosylation reactions this concept was introduced to the synthesis of photolabelled di- and trivalent mannosyl clusters.
 
Schlagworte:Mannosederivate ; carbohydrate-lectin interactions, thiourea bridging, photoaffinity labelling, glycosylation, FimH, mannosyl clusters, type-1-fimbriae, diazirine
 
Dokumente:
d931.pdf (12.242 kB)    ZIP generieren   Details >>