Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Pharmacy

Cyclotides are small cyclic plant proteins, and this thesis addresses their cytotoxic structure-activity properties and their mode of action on human cancer cell lines. Cyclotides were isolated from Viola odorata and Viola tricolor ; three novel cyclotide sequences and two known sequences, but of ne...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Svangård Erika 1975- , Uppsala universitet, Institutionen för läkemedelskemi, Svangård Erika 1975-, Uppsala University, Department of Pharmaceutical Chemistry
Format: Dissertation
Sprache:eng ; swe
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Cyclotides are small cyclic plant proteins, and this thesis addresses their cytotoxic structure-activity properties and their mode of action on human cancer cell lines. Cyclotides were isolated from Viola odorata and Viola tricolor ; three novel cyclotide sequences and two known sequences, but of new origin, were identified using mass spectrometry, amino acid analysis, and Edman degradation. The cyclotide structure includes three disulphide bonds in a knotted arrangement, which forces hydrophobic amino acid residues to be exposed on the surface of the molecule; 3-D homology models of cyclotides have revealed an amphipathic surface and charged residues located at similar positions in the molecules. The charged amino acid residues were shown to play a key role in the cytotoxicity of the cyclotide cycloviolacinO2 on a human lymphoma cell line. Methylation of Glu caused a dramatic change in cytotoxicity, lowering the potency 48 times, whereas concealing the charge of Arg with 1,2-cyclohexanedione caused virtually no change in potency. Acetylation of the two Lys caused a 3-fold reduction in potency, and masking all positive charges caused a 7-fold reduction. Additionally, disturbing the amphipathic structure by reducing and alkylating the disulphide bonds abolished the cytotoxicity. The time dependency of cytotoxicity and cell gross morphology after cyclotide exposure were investigated on the lymphoma cell line. Cells exposed to 4 µM of cycloviolacinO2 showed necrotic characteristics, such as membrane disintegration, within 5 min; a membrane disruptive effect of cycloviolacinO2 was also observed in a functional assay based on liposomes at a peptide-to-lipid molar ratio of 6.5. The anti-tumour properties of cycloviolacinO2 were evaluated on three human cancer cell lines using the hollow fibre assay in vitro and in vivo . The cyclotide exhibited potent anti-tumour activity in the micro-molar concentration range on all cell lines in vitro , but no effect on tumour growth could be established in vivo . Härtill 6 uppsatser Diss. (sammanfattning) Uppsala : Uppsala universitet, 2005 Docteur en pharmacie farmacie doktorsexamen degree of Doctor of Philosophy in Pharmacy Doctor pharmaciae Room C4:301, BMC, Uppsala Härtill 6 uppsatser Diss. (sammanfattning) Uppsala : Uppsala universitet, 2005 farmacie doktorsexamen Doctor pharmaciae Room C4:301, BMC, Uppsala Cyclotides are small cyclic plant proteins, and this thesis addresses their cytotoxic structure-activity properties