Solid-Phase Total Synthesis of Dehydrotryptophan-Bearing Cyclic Peptides Tunicyclin B, Sclerotide A, CDA3a and CDA4a using a Protected β-Hydroxytryptophan Building Block
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Date
2021-05-31
Authors
Diamandas, Matthew
Journal Title
Journal ISSN
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Publisher
University of Waterloo
Abstract
The non-proteinogenic amino acid Z-dehydrotryptophan can be found in a several
naturally occurring peptide. Amongst them are cyclic peptides such as tunicyclin B, the antifungal
agents keramamide F and sclerotide A, as well as the antibiotic telomycin and the calcium-dependent antibiotics (CDAs). Despite there being numerous means of accessing simple Z-dehydrotryptophan building blocks, it was only recently that the first synthesis of a Z-dehydrotryptophan peptide containing more than two amino acids was reported. However, the
synthetic method reported in this study is labor-intensive and not practical for rapid synthesis of
Z-dehydrotryptophan containing peptides.
In Chapter 2, a new and highly efficient approach to the synthesis of Z-dehydrotryptophan
peptides is initially described. This approach uses Fmoc-β-HOTrp(Boc)(TBS)-OH as a building
block, which is readily prepared in high yield and incorporated into peptides using solid-phase
Fmoc chemistry. The TBS-protected indolic alcohol eliminates during global deprotection/resin
cleavage to give Z-dehydrotryptophan peptides exclusively as the thermodynamically favored Z-isomer. This approach was applied to the solid-phase synthesis of tunicyclin B and sclerotide A
which were prepared in 28 % and 24 % overall yields respectively.
In Chapter 3, this method was used in the solid-phase synthesis of more challenging
targets which included biologically active CDA3a and CDA4a which were prepared in 6 % and 8.5
% overall yields respectively. Furthermore, using a similar solid-phase approach, two CDA
analogs, which contain either Trp or Kyn in place of the Z-dehydrotryptophan of CDA4a, were
prepared. The antibacterial potencies of CDA3a, CDA4a and these CDA analogs were assessed in
order to assemble a preliminary structure activity relation (SAR) study. Finally, early biological
studies were conducted on Z-dehydrotryptophan containing CDA4a in order to begin to decipher
the CDA’s biological mechanism of action (MoA).
Chapter 4 offers general conclusions about the work within this thesis. Furthermore, the
chapter presents recommendations for future work to be conducted in a continuation of the
findings outlined within this thesis. They include pursuing the synthesis of other, complex Z-dehydrotryptophan containing peptides as well as preparing further CDA analogs in order to
conduct a thorough SAR study on this class of compounds.
Description
Keywords
peptides, synthesis, antibiotics