Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Dynamic G-quadruplex supramolecular hydrogels have aroused great interest in a broad range of bioapplications. However, neither the development of native extracellular matrix (ECM)-derived natural biopolymer-functionalized G-quadruplex hydrogels nor their use to create perfusable self-supporting hydrogels has been explored to date, despite their intrinsic potential as carrier vehicles of therapeutic agents, or even living cells in advanced regenerative therapies, or as platforms to enable the diffusion of nutrients and oxygen to sustain long-term cell survival. Herein, we developed a dynamic co-assembling multicomponent system that integrates guanosine (G), 3-aminophenylboronic acid functionalized hyaluronic acid (HA-PBA), and potassium chloride to bioengineer strong, homogeneous, and transparent HA-functionalized G-quadruplex hydrogels with injectable, thermo-reversible, conductive, and self-healing properties. The supramolecular polymeric hydrogels were developed by hydrogen bonding and stacking interactions between G coupled dynamic covalent boronate ester bonds to HA-PBA and stabilized by K ions, as demonstrated by a combination of experiments and molecular dynamics simulations. The intrinsic instability of the self-assembled G-quadruplex structures was used to bioengineer self-supporting perfusable multicomponent hydrogels with interconnected size and shape-tunable hollow microchannels when embedded in 3D methacrylated gelatin supporting matrices. The microchannel-embedded 3D constructs have shown enhanced cell viability when compared to the bulk hydrogels, holding great promise for being use as artificial vessels for enabling the diffusion of nutrients and oxygen essential for cell survival. The proposed approach opens new avenues on the use of ECM-derived natural biopolymer-functionalized dynamic G-quadruplex hydrogels to design next-generation smart systems for being used in tissue regeneration, drug screening, or organ-on-a-chip.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336844PMC
http://dx.doi.org/10.1021/acs.biomac.3c00433DOI Listing

Publication Analysis

Top Keywords

g-quadruplex hydrogels
12
hydrogels
9
perfusable multicomponent
8
multicomponent hydrogels
8
dynamic g-quadruplex
8
ecm-derived natural
8
natural biopolymer-functionalized
8
diffusion nutrients
8
nutrients oxygen
8
cell survival
8

Similar Publications

In the motor neurons of amyotrophic lateral sclerosis (ALS) patients, excessive (G4C2)n repeats in the intronic region of the C9orf72 gene are transcribed to RNA, forming G-quadruplexes that sequester RNA-binding proteins, leading to gelation within the cytoplasm as one of the many mechanisms leading to pathogenesis. While ALS patients frequently harbor over 700 repeats, this kind of 100% GC-rich region is very difficult to clone, and past studies report the necessity to add additional sequences in the middle to clone more than a few dozen repeats. The goal of this study was the in vitro production of the longest repetitive RNA to date consisting solely of (G4C2)n repeats.

View Article and Find Full Text PDF

Recyclable G-quadruplex-driven hydrogel electrolyte for interface-compatible sustainable supercapacitors.

J Colloid Interface Sci

November 2025

Polymeric and Soft Materials Laboratory, School of Chemistry and Life Science and Advanced Institute of Materials Science, Changchun University of Technology, Changchun 130012, China. Electronic address:

Sustainable hydrogel-based supercapacitors are emerging as promising options for safe and green energy storage solutions, but suffer from low energy density and non-recyclability. Herein, a G-quadruplex-driven hydrogel electrolyte with recyclability and ion channels is successfully designed and applied to construct interface-compatible sustainable supercapacitors. The G-quadruplex-driven supramolecular network with ion channels not only enables hydrogel electrolytes to achieve high ionic conductivity, but also imparts thermally activated reversible regulation of network structure for the construction of interface-compatible supercapacitors.

View Article and Find Full Text PDF

A portable fluorescent aptamer sensor for rapid quantitative detection of Hg.

Anal Methods

May 2025

College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety and Nutrition, Zhengzhou, 450001, P. R. China.

Mercury(II) ions (Hg) are heavy metal ions that can cause human poisoning and can lead to death in severe cases. Therefore, establishing a rapid quantitative detection method for Hg is important for protecting human health. In this study, a portable hydrogel-based fluorescent aptasensor was developed for the rapid and quantitative detection of Hg.

View Article and Find Full Text PDF

The mixing of Guanosine (Gua) and Guanosine 5'-monophosphate (GMP) in water in selected compositions yields highly hydrated, transparent, and self-healing self-assembled supramolecular G-hydrogels, attractive for biomedical applications. This work investigates how hydrogel composition affects solute transport, including diffusion, binding, loading, and release properties, using a set of fluorescent probes with varying size and polarity. Although small/wide-angle X-ray scattering techniques showed that no structural changes are induced by probe addition, even when intercalation into G-quadruplexes is expected, the internal mesh structure of the hydrogel, modulated by the Gua:GMP ratio, directly impacts probe diffusivity and loading.

View Article and Find Full Text PDF

Self-Regulating Hydrogel with Reversible Optical Activity in Its Gel-to-Gel Transformation.

J Am Chem Soc

May 2025

Institute for Complex Molecular Systems and Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, Eindhoven 5600 MB, Netherlands.

This study reports a supramolecular gel system capable of dynamic gel-to-gel transformations and reversible inversion of optical activity between superhelical and single-helical structures without passing through a sol phase. Inspired by collagen-like adaptability, the system utilizes 4-pyridinylboronic acid and guanosine as building blocks. Hierarchical assembly is achieved through pH-responsive boronic ester formation and guanosine-mediated G-quadruplex stacking, enabling transitions between superhelices and single helices with opposite optical activity.

View Article and Find Full Text PDF