Eluted latest among the three disulfide scrambled isomers along the oxidative folding pathway consistent with it being the most stable form. The seeds of Cucurbitaceae species are emerging as a rich source of novel disulfide-rich peptides. In this study we Calicheamicin isolated two peptides from the seeds of M. charantia that contain novel sequences and ICK structural motifs. Analysis of the oxidative refolding highlighted a common intermediate present in the folding of a variety of ICK peptides, despite variations in Finafloxacin inter-cysteine loop sizes. This two-disulfide intermediate is surprisingly stable and provides new insights into how the cystine knot might have evolved from a simple disulfide framework. A comparison of the sequences of MCh-1 and MCh-2 with peptides isolated from the related species M. cochinchinensis shows that although the peptides all contain six cysteine residues, and loops 3 and 4 all contain the same number of residues, the other inter-cysteine loops are variable. Similarly, the sequences differ from the squash trypsin inhibitors isolated from Momordica species. These sequence differences are reflected in the different retention times observed on RP-HPLC, with the squash trypsin inhibitors being more hydrophilic than MCh-1 and MCh-2. The peptides also differ in activity, as MCh-1 and MCh-2 are not trypsin inhibitors. Given the differences in sequence and activity it is apparent these novel peptides belong to a new subfamily of ICK members. It is interesting to note the differences in retention times of the intermediates during the selective reduction and the stepwise alkylation, or the oxidative refolding and the stepwise alkylation. The intermediate IIa eluted just before the native peptide and the similarity of the retention times of the intermediate with that of the native peptide indicates that the three-dimensional structures are similar and that the intermediate also contains a compact structure. The retention time of NEM-alkylated IIa was almost the same as that of IIa. This similarity in retention times suggests that the NEM replacement did not affect the conformation of IIa. By contrast, the retention times of NEM-alkylated Ia, the fully alkylated MCh-1 and intermediate Ia decreased dramatically relative to the native peptide, which indicat
