: The ability of synthetic peptides inhibitors of NOX1 to effectively block the production of ROS by the enzyme was studied with different methodologies. Specifically, taking advantage of our understanding of the active epitope of the regulatory NOX1 subunit NOXA1 as a potent inhibitor of NOX1-derived O2•- formation, a panel of peptidomimetic derivatives of this peptide were designed and synthesized with the aim of improving their activity and increasing their stability in plasma. The results highlighted that improved efficacy and potency was found for both the peptide-peptoid hybrid GS2, whereas stapled peptide AC5 and its precursor showed higher stability despite lower biological potency. This study showed that minimal structural modifications of NOXA1 peptides are required to improve both their potency and stability to finally achieve best candidates as new potential anti-thrombotic drugs.

Development of new peptidomimetic NADPH oxidase inhibitors with antithrombotic properties / Scalia, Elisabetta; Chirco, Antony; Calugi, Lorenzo; Lenci, Elena; Pagano, Patrick J; Pula, Giordano; Trabocchi, Andrea. - In: CHEMMEDCHEM. - ISSN 1860-7179. - ELETTRONICO. - (2024), pp. 0-0. [10.1002/cmdc.202400330]

Development of new peptidomimetic NADPH oxidase inhibitors with antithrombotic properties

Scalia, Elisabetta;Chirco, Antony;Calugi, Lorenzo;Lenci, Elena;Trabocchi, Andrea
2024

Abstract

: The ability of synthetic peptides inhibitors of NOX1 to effectively block the production of ROS by the enzyme was studied with different methodologies. Specifically, taking advantage of our understanding of the active epitope of the regulatory NOX1 subunit NOXA1 as a potent inhibitor of NOX1-derived O2•- formation, a panel of peptidomimetic derivatives of this peptide were designed and synthesized with the aim of improving their activity and increasing their stability in plasma. The results highlighted that improved efficacy and potency was found for both the peptide-peptoid hybrid GS2, whereas stapled peptide AC5 and its precursor showed higher stability despite lower biological potency. This study showed that minimal structural modifications of NOXA1 peptides are required to improve both their potency and stability to finally achieve best candidates as new potential anti-thrombotic drugs.
2024
0
0
Scalia, Elisabetta; Chirco, Antony; Calugi, Lorenzo; Lenci, Elena; Pagano, Patrick J; Pula, Giordano; Trabocchi, Andrea
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1366292
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