Supramolecular multiplexes from collagen mimetic peptide-PNA(GGG)<sub>3</sub> conjugates and C-rich DNA: pH-induced reversible switching from triplex–duplex to triplex-<i>i</i>-motif
Peptides are well known for forming nanoparticles, while DNA duplexes, triplexes and tetraplexes create rigid nanostructures. Accordingly, the covalent conjugation of peptides to DNA/RNA produces hybrid self-assembling features and may lead to interesting nano-assemblies distinct from those of their individual components. Herein, we report the preparation of a collagen mimetic peptide incorporating lysine in its backbone, with alkylamino side chains radially conjugated with G-rich PNA [collagen-(PNA-GGG)<sub>3</sub>]. In the presence of complementary C-rich DNA (dCCCTTTCCC) at neutral pH, the collagen mimetic triplexes were interconnected by PNA-GGG : DNA-CCC duplexes, leading to the formation of larger assemblies of nanostructures. Upon decreasing the pH to 4.5, the dissociation of the triplex-duplex assembly released the protonated C-rich DNA, which immediately folded into an <i>i</i>-motif. With an increase in the pH to 7.2 (neutral), the <i>i</i>-motif unfolded into linear DNA, which reformed the PNA-GGG : DNA-CCC duplex interconnecting the collagen triplexes. The pH-induced switching of the assembly and disassembly was reversible over a few cycles. The hybrid collagen-(PNAGGG)<sub>3</sub> : DNA-C<sub>3</sub>T<sub>3</sub>C<sub>3</sub> triplex-duplex and the individual components of the assembly including the <i>i</i>-motif were characterized by UV and CD melting, fluorescence, TEM and gel electrophoresis. The pH-induced reversible switching was established by the changes in the CD and fluorescence properties. Peptide-DNA conjugates have wide applications in both biology and materials science, ranging from therapeutics and drug delivery to diagnostics and molecular switches. Thus, the prototype ensemble of the triplex peptide-PNA conjugate and its duplex with DNA described herein has potential for elaboration into rationally designed systems by varying the PNA/DNA sequences to trap functional ligands/drugs for release in pH-controlled environments.
Authors
- Krishna N. Ganesh (ORCID: https://orcid.org/0000-0003-2292-643X)
- Shahaji H. More (ORCID: https://orcid.org/0000-0002-0042-4052)
- Marc Schmutz (ORCID: https://orcid.org/0000-0003-4059-7609)
- Loı̈c Jierry (ORCID: https://orcid.org/0000-0002-7541-1360)
Institutions
- Centre National de la Recherche Scientifique (FR)
- Institut Charles Sadron (FR)
- Indian Institute of Science Education and Research, Tirupati (IN)
- Université de Strasbourg (FR)
Publication Details
- Journal
- Biomaterials Science
- Published
- 2024-10-25
- DOI
- https://doi.org/10.1039/d4bm00955j
- Citations
- 2
- Primary Topic
- Biopolymer Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- Indian Institute of Science Education and Research Pune
- Science and Engineering Research Board