Abstract
Axinastatin 3 as a potential anticancer agent was synthesized by chemical methods. In an electrospray ion-trap mass spectrometer, using one stage of tandem mass spectrometry (MS/MS), the linear peptide intermediate was sequenced via the complementarities of y and b ions. Then, using multistep MS/MS (to MS6), the cyclic peptide was sequenced through sequentially removing one amino acid residue in each stage of MS/MS. The difference of the fragmentation mechanisms and the sequencing approaches between them is discussed. © Versita Warsaw and Springer-Verlag Berlin Heidelberg 2006.
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Jia, C., Qi, W., He, Z., & Qiao, B. (2006). Sequencing peptides by electrospray ion-trap mass spectrometry: A useful tool in synthesis of Axinastatin 3. Central European Journal of Chemistry, 4(4), 620–631. https://doi.org/10.2478/s11532-006-0028-y
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