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The discovery of allyltyrosine based tripeptides as selective inhibitors of the HIV-1 integrase strand-transfer reaction

Journal Article


Abstract


  • From library screening of synthetic antimicrobial peptides, an O-allyltyrosine-based tripeptide was identified to possess inhibitory activity against HIV-1 integrase (IN) exhibiting an IC50 value of 17.5 μM in a combination 3′-processing and strand transfer microtitre plate assay. The tripeptide was subjected to structure–activity relationship (SAR) studies with 28 peptides, incorporating an array of natural and non-natural amino acids. Resulting SAR analysis revealed the allyltyrosine residue was a key feature for IN inhibitory activity whilst incorporation of a lysine residue and extended hydrophilic chains bearing a terminal methyl ester was advantageous. Addition of hydrophobic aromatic moieties to the N-terminal of the scaffold afforded compounds with improved inhibitory activity. Consolidation of these functionalities lead to the development of the tripeptide 96 which specifically inhibited the IN strand-transfer reaction with an IC50 value of 2.5 μM.

Authors


  •   Dalton, Neal (external author)
  •   Gordon, Christopher P. (external author)
  •   Boyle, Timothy (external author)
  •   Vandegraaff, Nicholas (external author)
  •   Deadman, John (external author)
  •   Rhodes, David I. (external author)
  •   Coates, Jonathon A. (external author)
  •   Pyne, Stephen G.
  •   Keller, Paul A.
  •   Bremner, John B.

Publication Date


  • 2016

Citation


  • Dalton, N., Gordon, C. P., Boyle, T. P., Vandegraaff, N., Deadman, J., Rhodes, D. I., Coates, J. A., Pyne, S. G., Keller, P. A. & Bremner, J. B. (2016). The discovery of allyltyrosine based tripeptides as selective inhibitors of the HIV-1 integrase strand-transfer reaction. Organic and Biomolecular Chemistry, 14 (25), 6010-6023.

Scopus Eid


  • 2-s2.0-84975810851

Number Of Pages


  • 13

Start Page


  • 6010

End Page


  • 6023

Volume


  • 14

Issue


  • 25

Abstract


  • From library screening of synthetic antimicrobial peptides, an O-allyltyrosine-based tripeptide was identified to possess inhibitory activity against HIV-1 integrase (IN) exhibiting an IC50 value of 17.5 μM in a combination 3′-processing and strand transfer microtitre plate assay. The tripeptide was subjected to structure–activity relationship (SAR) studies with 28 peptides, incorporating an array of natural and non-natural amino acids. Resulting SAR analysis revealed the allyltyrosine residue was a key feature for IN inhibitory activity whilst incorporation of a lysine residue and extended hydrophilic chains bearing a terminal methyl ester was advantageous. Addition of hydrophobic aromatic moieties to the N-terminal of the scaffold afforded compounds with improved inhibitory activity. Consolidation of these functionalities lead to the development of the tripeptide 96 which specifically inhibited the IN strand-transfer reaction with an IC50 value of 2.5 μM.

Authors


  •   Dalton, Neal (external author)
  •   Gordon, Christopher P. (external author)
  •   Boyle, Timothy (external author)
  •   Vandegraaff, Nicholas (external author)
  •   Deadman, John (external author)
  •   Rhodes, David I. (external author)
  •   Coates, Jonathon A. (external author)
  •   Pyne, Stephen G.
  •   Keller, Paul A.
  •   Bremner, John B.

Publication Date


  • 2016

Citation


  • Dalton, N., Gordon, C. P., Boyle, T. P., Vandegraaff, N., Deadman, J., Rhodes, D. I., Coates, J. A., Pyne, S. G., Keller, P. A. & Bremner, J. B. (2016). The discovery of allyltyrosine based tripeptides as selective inhibitors of the HIV-1 integrase strand-transfer reaction. Organic and Biomolecular Chemistry, 14 (25), 6010-6023.

Scopus Eid


  • 2-s2.0-84975810851

Number Of Pages


  • 13

Start Page


  • 6010

End Page


  • 6023

Volume


  • 14

Issue


  • 25