Bio-inspired membrane design unlocks new possibilities for water purification, extraction
Peer-Reviewed Publication
Updates every hour. Last Updated: 1-Jan-2026 21:11 ET (2-Jan-2026 02:11 GMT/UTC)
Researchers from the University of Chicago Pritzker School of Molecular Engineering and Northwestern University have turned to biology to potentially revolutionize how people make water safe to drink and remove harmful – or valuable – chemicals from oceans, lakes and rivers. Cell membranes selectively let in more ions of life-sustaining materials like potassium or sodium when the cell needs them and can shut off the flow before the chemical concentration gets too high. Inspired by this, the team fabricated angstrom-scale artificial solid ionic channels aiming to replicate these biological ion channels. By adding different amounts of lead, cobalt or barium ions, the team found it could vastly increase or limit the amount of potassium passing through an artificial membrane, mimicking cells’ abilities to act as their own biochemical bouncers. Among the team’s more remarkable findings was that just a 1% increase in the presence of lead ions doubled the amount of potassium coming through the channels.
A research team has successfully engineered Corynebacterium glutamicum into a versatile cell factory capable of producing a wide range of biochemicals, including amino acids, organic acids, alcohols, terpenoids, and biopolymers.
A research team engineered thymidine auxotrophic and recombination-deficient versions of commonly used and underutilized Agrobacterium strains, using single-component CRISPR base-editing systems.
Scientists have corrected gene mutations in mice causing an ultra-rare disease by editing DNA directly in the brain with a single injection, a feat with profound implications for patients with neurological diseases. In tests that also included patient derived cells, the cutting-edge technique not only fixed mutations causing alternating hemiplegia in childhood (AHC) — it also reduced symptoms and extended survival in mice that had AHC and were otherwise at risk of sudden death. The findings were published in Cell.
Researchers at the Broad Institute and The Jackson Laboratory have used prime editing, a precise and versatile form of gene editing, to correct the root cause of alternating hemiplegia of childhood (AHC), a debilitating genetic condition, in mice. The team used a scalable approach to develop prime editing treatments that directly repaired five different AHC-causing genetic mutations. Mice that received the treatment had far fewer and less severe symptoms of AHC, and survived more than twice as long as untreated mice.
Hydrogen peroxide (H2O2) is a versatile oxidant widely used in pharmaceuticals, environmental protection, and chemical manufacturing. However, conventional H2O2 production relies on energy-intensive processes and costly metal-based catalysts, raising economic and environmental concerns. As a sustainable alternative, photocatalytic H2O2 synthesis harnesses solar energy, water, and oxygen under mild conditions. This research group summarizes recent advancements in the development of metal-free organic semiconductors for photocatalytic H2O2 generation. Notably, it delves into novel surface reaction mechanisms, including anthraquinone intermediate, peroxy acid intermediate, bipyridine intermediate, and dual channel synergistic mechanisms for optimizing photocatalyst performance. They also highlight the critical role of advanced characterization techniques, including in-situ characterizations and computational simulations, in understanding structure-property relationships and real-time catalytic processes. By proposing new strategies for material modification and potential device-based applications, this review aims to stimulate further research and promote the industrialization of photocatalytic H2O2 production, contributing to sustainable chemical processes.
The application of CAR-T cell therapy against solid tumors is often hindered by the dense and rigid tumor extracellular matrix (ECM). While combining CAR-T with hyaluronidase (HAase) to reduce ECM is apparent, the efficacy is limited because of low accumulation and penetration efficiency of HAase inside the tumor tissue. Herein, the stimuli-responsive HAase-loaded nanogels (H-NGs) which are conjugated on the surface of CAR-T cells were designed for synergistically improving HAase accumulation, ECM degradation and CAR-T cell efficacy. The conjugation of H-NGs on the T cell surface was achieved through metabolic oligosaccharide engineering (MOE) in a semi-quantitatively controlled manner. Intravenous injection of H-NGs armed CAR-T cells resulted in more ECM degradation than co-injection of CAR-T cells and free H-NGs, leading to an 83.2% tumor inhibition rate and relieves tumor suppressive microenvironment in the Raji solid tumor model. Proteomic analysis of the harvested tumor tissues indicated that the combining of H-NGs and CAR-T cell collaboratively reduces cell adhesion and enhanced leukocyte transendothelial migration. Overall, this work simultaneously boosts the efficacy of hyaluronidase and CAR-T cells in combating solid tumor, which has broad application potential in cancer combination therapy.