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Updated: Jun 20, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
Published on: March 25, 2014
Potent inhibitors of beta-tryptase and human leukocyte elastase based on the MCoTI-II scaffold
Panumart Thongyoo1, Camille Bonomelli, Robin J Leatherbarrow
1Department of Chemistry and Chemical Biology Centre, Imperial College London SW7 2AZ, UK.
Abstract:
MCoTI-II is a member of a class of microproteins known as cyclotides that possess a macrolactam-cystine knot scaffold imparting exceptional physiological stability and structural rigidity. Modification of residues in the active loop and engineered truncations have resulted in MCoTI-II analogues that possess potent activity against two therapeutically significant serine proteases: beta-tryptase and human leukocyte elastase. These results suggest that MCoTI-II is a versatile scaffold for the development of protease inhibitors against targets in inflammatory disease.
