Home LiteratureArticle Details
PMID: 18191970 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The alpine violet, Viola biflora, is a rich source of cyclotides with potent cytotoxicity.

Phytochemistry ·Vol. 69 ·No. 4 ·2008-02-00 ·Pages 939-52

Herrmann A, Burman R, Mylne JS, Karlsson G, Gullbo J, Craik DJ, Clark RJ, Göransson U

Abstract

The cyclotides are currently the largest known family of head-to-tail cyclic proteins. The complex structure of these small plant proteins, which consist of approximately 30 amino acid residues, contains both a circular peptide backbone and a cystine knot, the combination of which produces the cyclic cystine knot motif. To date, cyclotides have been found in plants from the Rubiaceae, Violaceace and Cucurbitaceae families, and are believed to be part of the host defence system. In addition to their insecticidal effect, cyclotides have also been shown to be cytotoxic, anti-HIV, antimicrobial and haemolytic agents. In this study, we show that the alpine violet Viola biflora (Violaceae) is a rich source of cyclotides. The sequences of 11 cyclotides, vibi A-K, were determined by isolation and MS/MS sequencing of proteins and screening of a cDNA library of V. biflora in parallel. For the cDNA screening, a degenerate primer against a conserved (AAFALPA) motif in the cyclotide precursor ER signal sequence yielded a series of predicted cyclotide sequences that were correlated to those of the isolated proteins. There was an apparent discrepancy between the results of the two strategies as only one of the isolated proteins could be identified as a cDNA clone. Finally, to correlate amino acid sequence to cytotoxic potency, vibi D, E, G and H were analysed using a fluorometric microculture cytotoxicity assay using a lymphoma cell line. The IC(50)-values of the bracelet cyclotides vibi E, G and H ranged between 0.96 and 5.0 microM while the Möbius cyclotide vibi D was not cytotoxic at 30 microM.

MeSH Terms
Amino Acid Sequence Cell Line, Tumor Cell Survival/drug effects Cyclotides/chemistry,metabolism,toxicity Humans Molecular Sequence Data Protein Structure, Secondary Sequence Homology, Amino Acid Tandem Mass Spectrometry Viola/genetics,metabolism
Chemicals
Cyclotides
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Herrmann Anders
Division of Pharmacognosy, Department of Medicinal Chemistry, Uppsala University, Biomedical Centre, P.O. Box 574, SE-751 23 Uppsala, Sweden.
Burman Robert
Mylne Joshua S
Karlsson Gustav
Gullbo Joachim
Craik David J
Clark Richard J
Göransson Ulf
Article Info
Journal
Phytochemistry
Abbr.
Phytochemistry
ISSN
0031-9422
Published
2008-02-00
Epub
2008-00-14
Pages
939-52
Language
English
Region
England
NLM ID
0151434
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com