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Structure and biological evaluation of new cyclic and acyclic laxaphycin-A type peptides.

Abstract
Five new laxaphycins were isolated and fully characterised from the bloom forming cyanobacteria Anabaena torulosa sampled from Moorea, French Polynesia: three acyclic laxaphycin A-type peptides, acyclolaxaphycin A (1), [des-Gly11]acyclolaxaphycin A (2) and [des-(Leu10-Gly11)]acyclolaxaphycin A (3), as well as two cyclic ones, [l-Val8]laxaphycin A (4) and [d-Val9]laxaphycin A (5). The absolute configuration of the amino acids, established using advanced Marfey's analysis for compounds 2-5, highlights a conserved stereochemistry at the Cα carbons of the peptide ring that is characteristic of this family. To the best of our knowledge, this is the first report of acyclic analogues within the laxaphycin A-type peptides. Whether these linear laxaphycins with the aliphatic β-amino acid on the N-terminal are biosynthetic precursors or compounds obtained after enzymatic hydrolysis of the macrocycle is discussed. Biological evaluation of the new compounds together with the already known laxaphycin A shows that [l-Val8]laxaphycin A, [d-Val9]laxaphycin A and [des-Gly11]acyclolaxaphycin induce cellular toxicity whereas laxaphycin A and des-[(Leu10-Gly11)]acyclolaxaphycin A do not affect the cellular viability. An analysis of cellular death shows that the active peptides do not induce apoptosis or necrosis but instead, involve the autophagy pathway.
AuthorsLouis Bornancin, Eva Alonso, Rebeca Alvariño, Nicolas Inguimbert, Isabelle Bonnard, Luis M Botana, Bernard Banaigs
JournalBioorganic & medicinal chemistry (Bioorg Med Chem) Vol. 27 Issue 10 Pg. 1966-1980 (05 15 2019) ISSN: 1464-3391 [Electronic] England
PMID30929947 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2019 Elsevier Ltd. All rights reserved.
Chemical References
  • Laxaphycin A
  • Peptides
  • Peptides, Cyclic
  • Reactive Oxygen Species
Topics
  • Anabaena (metabolism)
  • Apoptosis (drug effects)
  • Cell Line, Tumor
  • Humans
  • Membrane Potential, Mitochondrial (drug effects)
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptides (chemistry, pharmacology)
  • Peptides, Cyclic (chemistry, pharmacology)
  • Protein Conformation
  • Reactive Oxygen Species (metabolism)

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