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Motivation Enzymatic reaction play a pivotal role in regulating cellular processes with a high degree of specificity to biological functions. When enzymatic reactions are disrupted by gene, protein, or metabolite dysfunctions in diseases, it becomes crucial to visualize the resulting perturbed enzymatic reaction-induced multi-omics network. Multi-omics network visualization aids in gaining a comprehensive understanding of the functionality and regulatory mechanisms within biological systems. Results In this study, we designed PhenoMultiOmics, an enzymatic reaction-based multi-omics web server designed to explore the scope of the multi-omics network across various cancer types. We first curated the PhenoMultiOmics database, which enables the retrieval of cancer-gene–protein-metabolite relationships based on the enzymatic reactions. We then developed the MultiOmics network visualization module to depict the interplay between genes, proteins, and metabolites in response to specific cancer-related enzymatic reactions. The biomarker discovery module facilitates functional analysis through differential omic feature expression and pathway enrichment analysis. PhenoMultiOmics has been applied to analyze the transcriptomics data of gastric cancer and the metabolomics data of lung cancer, providing mechanistic insights into interrupted enzymatic reactions and the associated multi-omics network. Availability and implementation PhenoMultiOmics is freely accessed at https://phenomultiomics.shinyapps.io/cancer/ with a user-friendly and interactive web interface. [ABSTRACT FROM AUTHOR]

The manipulation of trap states plays a crucial role in the development of efficient photocatalysts. An ultrathin-shelled Zn-AgIn5S8/ZnS quantum dots (QDs) photocatalyst was synthesized via in situ growth using a low-temperature hydrothermal method. The optical properties of the samples coated with ZnS shell were studied vis UV-vis absorption and fluorescence spectra. The ultrathin ZnS shell plays an important role in the Zn-AgIn5S8/ZnS core–shell heterostructure photocatalytic water splitting system, which could reduce surface defects, prolong the carrier lifetime and improve the photo-generated electron–hole pair separation effectively, resulting in the improved photocatalytic efficiency and enhanced stability of the catalyst. The results provide an effective guideline for shell thickness design in future constructions of the core–shell heterostructure photocatalyst. [ABSTRACT FROM AUTHOR]

Exploring low-cost and high-performance oxygen evolution reaction (OER) catalysts has attracted great attention due to their crucial role in water splitting. Here, a bifunctional Cu 5 FeS 4 /Ni 3 S 2 @NF catalyst was in situ formed on a nickel (Ni) foam toward efficient photoassisted electrocatalytic (P-EC) OER, which displays an ultralow overpotential of 260 mV at 30 mA cm -2 in alkaline solution, outperforming most previously reported Ni-based catalysts. It also shows great potential in degradation of antibiotics as an alternative anode reaction to OER owing to the prompt transfer of photogenerated holes. The photocurrent test and transient photovoltage spectroscopy indicate that the synergistic coupling of charge extraction and sinking effects in Cu 5 FeS 4 and Ni 3 S 2 is critical for boosting the OER activity via photoassistance. Electrochemical active surface area and electrochemical impedance spectroscopy tests further prove that the photogenerated electromotive force can effectively compensate the overpotential of OER. This work not only provides a good guidance for integrating photocatalysis and electrocatalysis, but also indicates the key role of synergistic extraction and utilization of photogenerated charge carriers in P-EC.