Authors
Johannes Koehbach, Margaret O’Brien, Markus Muttenthaler, Marion Miazzo, Muharrem Akcan, Alysha G Elliott, Norelle L Daly, Peta J Harvey, Sarah Arrowsmith, Sunithi Gunasekera, Terry J Smith, Susan Wray, Ulf Göransson, Philip E Dawson, David J Craik, Michael Freissmuth, Christian W Gruber
Publication date
2013/12/24
Journal
Proceedings of the National Academy of Sciences
Volume
110
Issue
52
Pages
21183-21188
Publisher
National Academy of Sciences
Description
Cyclotides are plant peptides comprising a circular backbone and three conserved disulfide bonds that confer them with exceptional stability. They were originally discovered in Oldenlandia affinis based on their use in traditional African medicine to accelerate labor. Recently, cyclotides have been identified in numerous plant species of the coffee, violet, cucurbit, pea, potato, and grass families. Their unique structural topology, high stability, and tolerance to sequence variation make them promising templates for the development of peptide-based pharmaceuticals. However, the mechanisms underlying their biological activities remain largely unknown; specifically, a receptor for a native cyclotide has not been reported hitherto. Using bioactivity-guided fractionation of an herbal peptide extract known to indigenous healers as “kalata-kalata,” the cyclotide kalata B7 was found to induce strong contractility on human …
Total citations
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Scholar articles
J Koehbach, M O'Brien, M Muttenthaler, M Miazzo… - Proceedings of the National Academy of Sciences, 2013