FFC#11/2017

Development of a peptide derived from the enzyme PI3Kγ as a new and effective potentiator of the mutant F508del-CFTR

FFC#11/2017

Development of a peptide derived from the enzyme PI3Kγ as a new and effective potentiator of the mutant F508del-CFTR

PRINCIPAL INVESTIGATOR

Alessandra Ghigo (Dipartimento di Biotecnologie Molecolari e Scienze per la Salute, Università degli Studi di Torino)

RESEARCHERS

7

CATEGORY

AREA 1 Therapies to correct the underlying defect

DURATION

1 year

GOAL

€ 60.000 €

RESULTS

In the view of developing PI3Kγ peptide as a novel, human medicinal product researchers completed the chemical optimization of the peptide lead so that to obtain a molecule that recapitulates the biological features of the parent peptide but implying lower cost of synthesis. They identified the minimal active sequence (MIN seq) of PI3Kγ peptide fitted with these properties. Further, they investigated the molecular mechanisms underlying the ability of the parent PI3Kγ peptide to rescue F508del-CFTR function. Chloride current measurements and surface biotinylation assays were carried out in bronchial primary CF and CFBE41o- cells and the resulting data suggest that the PI3Kγ peptide exerts both corrective and potentiating effects and may be exploited as a single agent for the treatment of F508del defect. The PI3Kγ-derived peptide received the Orphan Drug Designation by the European Medicinal Agency (EU/3/17/1859) in 2017 and further studies will be carried out in regard to its preclinical safety assessment.


Congress abstracts

– Ghigo A, Murabito A, Ren K et al. “Development of a PI3Kγ-derived peptide as a standalone therapy to activate F508del-CFTR, limit lung inflammation and promote bronchorelaxation in Cystic Fibrosis” 15th ECFS Basic Science Conference – Loutraki (Greece) – March 21-24, 2018
– Murabito A, Ren K, Pirozzi F et al. “Exploiting a PI3Kγ Mimetic Peptide as a standalone drug to restore CFTR function, reduce inflammation and limit obstruction of the respiratory tract in cystic fibrosis” SIBBM 2018, Frontiers in Molecular Biology, Rome, Italy, June 20-22, 2018
– Murabito A, Ren K, Pirozzi F et al. “Exploiting a PI3Kγ Mimetic Peptide as a standalone drug to restore CFTR function, reduce inflammation and limit obstruction of the respiratory tract in cystic fibrosis” 15th ECFS Basic Science Conference – Loutraki (Greece) – March 21-24, 2018
– Murabito A, Ren K, Melotti P et al. “Exploiting a PI3KI mimetic peptide as a single molecule with three independent therapeutic benefits in cystic fibrosis” North American Cystic Fibrosis Conference (NACF), October 18-20, 2018, Denver, CO, USA

OTHER RESULTS

FFC #3/2024

Two molecules are effective in activating Heat Shock Proteins and enhancing the action of CFTR correctors with the F508del mutation in vitro.

FFC#5/2024

Some peptide nucleic acids (PNAs) re-sensitise Pseudomonas aeruginosa to the antibiotic meropenem in vitro and reduce its virulence.

FFC#1/2023

Tezacaftor, one of the components of Kaftrio, induces an accumulation of dihydroceramides both in vitro and in vivo in animal models