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In-silico Molecular Interaction of Short Synthetic Lipopeptide/Importin-alpha and In-vitro Evaluation of Transgene Expression Mediated by Liposome- Based Gene Carrier

Author(s):

Tarwadi Tarwadi*, Jalal A. Jazayeri, Sabar Pambudi, Alfan D. Arbianto, Heni Rachmawati, Rahmana E. Kartasasmita and Sukmadjaja Asyarie   Pages 1 - 12 ( 12 )

Abstract:


Background: Lipopeptide-based gene carriers have shown low cytotoxicity, are capable in cell membrane penetration, are easy to manufacture and therefore are great potential candidates for gene delivery applications.

Objectives: This study aims to explore a range of short synthetic lipopeptides, (Lau: Lauryl; Pal: Palmitoyl) consisting of an alkyl chain, one cysteine (C), 1 to 2 histidine (H), and lysine (K) residues by performing in-silico molecular interaction and in-vitro evaluation.

Methods: The molecular interactions between the lipopeptides and Importin-α receptor were performed using AutoDock Vina and Amber14. The lipopeptide/DNA complexes were evaluated in-vitro for their interactions, particle size, zeta potential and transgene expression. Transfection efficiency of the lipopeptides and Pal-CKKHH-derived liposome was carried out based on luciferase transgene expression.

Results: The in-silico interaction showed that Lau-CKKH and Pal-CKKHH hypothetically expedited nuclear uptake. Both lipopeptides had lower binding energy (-6.3 kcal/mol and -6.2 kcal/mol, respectively), compared to the native ligand, viz, nuclear localization sequence (-5.4 kcal/mol). The short lipopeptides were able to condense DNA molecules and efficiently and formed compacted nanoparticles. Based on in-vitro evaluation on COS-7, Pal-CKKHH was found to be the best transfection agent amongst the lipopeptides. It transfection efficiency (ng Luc/mg total protein) increased up to ~3-fold higher (1163 + 55) as it was formulated with helper lipid DOPE (1:2). The lipopeptide-based liposome (Pal-CKKHH: DOPE=1:2) also facilitated luciferase transgene expression on human embryonic kidney cells (293T) and human cervical adenocarcinoma cells (HeLa) with transfection efficiency 1779 +52 and 260 + 22, respectively.

Conclusion: Our study for the first time has shown that the fully synthesized short lipopeptide Pal-CKKHH is able to interact firmly with the Importin-α he lipopeptide is able to condense DNA molecules efficiently, facilitate transgene expression, expedite nuclear uptake process, and hence has the characteristics of a potential transfection agent.

Keywords:

lipopeptide, Importin- α in-silico, liposome, particle size, transfection.

Affiliation:

School of Pharmacy, Bandung Institute of Technology, Bandung 40132, School of Biomedical Sciences, Faculty of Science-Charles Sturt University, Wagga-Wagga, New South Wales 2678, Centre for Pharmaceutical and Medical Technology-BPPT, Jakarta 10340, Centre for Pharmaceutical and Medical Technology-BPPT, Jakarta 10340, School of Pharmacy, Bandung Institute of Technology, Bandung 40132, School of Pharmacy, Bandung Institute of Technology, Bandung 40132, School of Pharmacy, Bandung Institute of Technology, Bandung 40132



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