Molecular engineering of complexation between RNA and biodegradable cationic gemini surfactants: role of the hydrophobic chain length. Issue 5 (23rd February 2022)
- Record Type:
- Journal Article
- Title:
- Molecular engineering of complexation between RNA and biodegradable cationic gemini surfactants: role of the hydrophobic chain length. Issue 5 (23rd February 2022)
- Main Title:
- Molecular engineering of complexation between RNA and biodegradable cationic gemini surfactants: role of the hydrophobic chain length
- Authors:
- Akram, Mohd.
Lal, Hira
Shakya, Sonam
Varshney, Rohit
Kabir-ud-Din, - Abstract:
- Abstract : The effects of the hydrophobic alkyl chain length of C m -E2O-C m gemini surfactants ( m = 12, 14 and 16) on ribonucleic acid were investigated using different methods. The various calculated parameters revealed that complexation occurs via an intercalative binding mode. Abstract : The transfection efficiency of a material into cells is directly related to the success rate of gene therapy. Synthetic lipid-like molecules, comparable with the components of biological membranes, are used for this purpose due to their high effectiveness and low toxicity. In gene therapy, cationic gemini surfactants have shown great promise as delivery system components for genetic material due to their favorable physicochemical properties (low toxicity, low critical micelle concentration (CMC), and positive head groups). In this study, we investigated the complexation of ribonucleic acid (RNA) with three ester-based cationic C m -E2O-C m gemini surfactants with different hydrophobic alkyl chain lengths ( m = 12, 14, and 16). The various studies revealed that gemini surfactants (C16 -E2O-C16 ) with longer alkyl chains excellently interact with RNA and form stable complexes with 1 : 1 binding stoichiometry. Therefore, competitive displacement studies utilizing different dyes (ethidium bromide (EB), acridine orange (AO), and Hoechst 33258 HO) demonstrated binding through an intercalation mode, which was further confirmed via ultraviolet-visible (UV-vis) spectroscopy, circular dichroismAbstract : The effects of the hydrophobic alkyl chain length of C m -E2O-C m gemini surfactants ( m = 12, 14 and 16) on ribonucleic acid were investigated using different methods. The various calculated parameters revealed that complexation occurs via an intercalative binding mode. Abstract : The transfection efficiency of a material into cells is directly related to the success rate of gene therapy. Synthetic lipid-like molecules, comparable with the components of biological membranes, are used for this purpose due to their high effectiveness and low toxicity. In gene therapy, cationic gemini surfactants have shown great promise as delivery system components for genetic material due to their favorable physicochemical properties (low toxicity, low critical micelle concentration (CMC), and positive head groups). In this study, we investigated the complexation of ribonucleic acid (RNA) with three ester-based cationic C m -E2O-C m gemini surfactants with different hydrophobic alkyl chain lengths ( m = 12, 14, and 16). The various studies revealed that gemini surfactants (C16 -E2O-C16 ) with longer alkyl chains excellently interact with RNA and form stable complexes with 1 : 1 binding stoichiometry. Therefore, competitive displacement studies utilizing different dyes (ethidium bromide (EB), acridine orange (AO), and Hoechst 33258 HO) demonstrated binding through an intercalation mode, which was further confirmed via ultraviolet-visible (UV-vis) spectroscopy, circular dichroism (CD), and melting and viscosity measurement results. Moreover, in silico studies are consistent with the experimental results in terms of how the gemini surfactants bind RNA. … (more)
- Is Part Of:
- Molecular Systems Design and Engineering. Volume 7:Issue 5(2022)
- Journal:
- Molecular Systems Design and Engineering
- Issue:
- Volume 7:Issue 5(2022)
- Issue Display:
- Volume 7, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 5
- Issue Sort Value:
- 2022-0007-0005-0000
- Page Start:
- 487
- Page End:
- 506
- Publication Date:
- 2022-02-23
- Subjects:
- Chemistry -- Molecular aspects -- Periodicals
Chemical engineering -- Molecular aspects -- Periodicals
Nanotechnology -- Periodicals
620.5 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/me#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1me00147g ↗
- Languages:
- English
- ISSNs:
- 2058-9689
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.856400
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21579.xml