A Thermodynamic Study on the Interaction between RH-23 Peptide and DMPC-Based Biomembrane Models

ABSTRACT: Investigation of the interaction between drugs and biomembrane models, as a strategy to study and eventually improve drug/substrate interactions, is a crucial factor in preliminary screening. Synthesized peptides represent a source of potential anticancer and theragnostic drugs. In this st...

Full description

Autores:
Giordani Giordani, Cristiano
Russo, Stefano
Torrisi, Cristina
Morante, Silvia
Castelli, Francesco
Grazia Sarpietro, Maria
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/39538
Acceso en línea:
https://hdl.handle.net/10495/39538
Palabra clave:
Rastreo Diferencial de Calorimetría
Calorimetry, Differential Scanning
Dimiristoilfosfatidilcolina
Dimyristoylphosphatidylcholine
Péptidos
Peptides
Anticarcinógenos
Anticarcinogenic Agents
https://id.nlm.nih.gov/mesh/D002152
https://id.nlm.nih.gov/mesh/D004134
https://id.nlm.nih.gov/mesh/D010455
https://id.nlm.nih.gov/mesh/D016588
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Investigation of the interaction between drugs and biomembrane models, as a strategy to study and eventually improve drug/substrate interactions, is a crucial factor in preliminary screening. Synthesized peptides represent a source of potential anticancer and theragnostic drugs. In this study, we investigated the interaction of a novel synthesized peptide, called RH-23, with a simplified dimyristoylphosphatidylcholine (DMPC) model of the cellular membrane. The interaction of RH-23 with DMPC, organized either in multilamellar vesicles (MLVs) and in Langmuir-Blodgett (LB) monolayers, was assessed using thermodynamic techniques, namely differential scanning calorimetry (DSC) and LB. The calorimetric evaluations showed that RH-23 inserted into MLVs, causing a stabilization of the phospholipid gel phase that increased with the molar fraction of RH-23. Interplay with LB monolayers revealed that RH-23 interacted with DMPC molecules. This work represents the first experimental thermodynamic study on the interaction between RH-23 and a simplified model of the lipid membrane, thus providing a basis for further evaluations of the effect of RH-23 on biological membranes and its therapeutic/diagnostic potential.