Organic/inorganic heterostructures templated by interfacial instability-driven BCP colloids in deformable emulsion droplets.

Hybrid heterostructure materials have received considerable attention due to the integration of each component and abundant functional applications in micromotors, catalysis, photothermal therapy, drug delivery, and bioimaging. However, the preparation of organic/inorganic heterostructure nanoparticles (HSNPs) with high quality still remains a remarkable challenge since thermodynamically metastable structures usually coexist, resulting in a lack of organic scaffolds with extreme uniformity both in shape and size distribution. Here, we prepared polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) block copolymer (BCP) core-shell spherical colloids driven by interfacial instability of soft and deformable emulsion droplets. Ultra-low interfacial tension was achieved through the co-adsorption of BCP segments and sodium dodecyl sulfate (SDS) surfactant, which had a strong affinity with the P4VP segment at the interface of the emulsified droplets. The excellent and homogeneous BCP colloids were further utilized as organic scaffolds to selectively grow a functional SiO2 layer on the surface of the BCP spherical colloids, producing BCP/SiO2 HSNPs with highly uniform shape and size distribution originating from the PS-b-P4VP scaffolds, thus providing an efficient and general strategy to construct and design organic/inorganic HSNPs with diverse applications.

Unveiling the bioinformatic genes and their involved regulatory mechanisms in type 2 diabetes combined with osteoarthritis.

Background: Type 2 Diabetes Mellitus (T2D) and Osteoarthritis (OA) are both prevalent diseases that significantly impact the health of patients. Increasing evidence suggests that there is a big correlation between T2D and OA, but the molecular mechanisms remain elusive. The aims of this study are to investigate the shared biomarkers and potential molecular mechanisms in T2D combined with OA. Methods: T2D and OA-related differentially expressed genes (DEGs) were identified via bioinformatic analysis on Gene Expression Omnibus (GEO) datasets GSE26168 and GSE114007 respectively. Subsequently, extensive target prediction and network analysis were finished with Gene Ontology (GO), protein-protein interaction (PPI), and pathway enrichment with DEGs. The transcription factors (TFs) and miRNAs coupled in co-expressed DEGs involved in T2D and OA were predicted as well. The key genes expressed both in the clinical tissues of T2D and OA were detected with western blot and qRT-PCR assay. Finally, the most promising candidate compounds were predicted with the Drug-Gene Interaction Database (DGIdb) and molecular docking. Results: In this study, 209 shared DEGs between T2D and OA were identified. Functional analysis disclosed that these DEGs are predominantly related to ossification, regulation of leukocyte migration, extracellular matrix (ECM) structural constituents, PI3K/AKT, and Wnt signaling pathways. Further analysis via Protein-Protein Interaction (PPI) analysis and validation with external datasets emphasized MMP9 and ANGPTL4 as crucial genes in both T2D and OA. Our findings were validated through qRT-PCR and Western blot analyses, which indicated high expression levels of these pivotal genes in T2D, OA, and T2D combined with OA cases. Additionally, the analysis of Transcription Factors (TFs)-miRNA interactions identified 7 TFs and one miRNA that jointly regulate these important genes. The Receiver Operating characteristic (ROC) analysis demonstrated the significant diagnostic potential of MMP9 and ANGPTL4.Moreover, we identified raloxifene, ezetimibe, and S-3304 as promising agents for patients with both T2D and OA. Conclusion: This study uncovers the shared signaling pathways, biomarkers, potential therapeutics, and diagnostic models for individuals suffering from both T2D and OA. These findings not only present novel perspectives on the complex interplay between T2D and OA but also hold significant promise for improving the clinical management and prognosis of patients with this concurrent condition.

Scanning tunneling microscopy study of α,ω-dihexylsexithiophene adlayers on Au(111): a chiral separation induced by a surface.

The self-assembly of α,ω-dihexylsexithiophene molecules on an Au(111) surface was examined by using scanning tunneling microscopy at room temperature, revealing the internal molecular structures of the sexithiophene backbones and the hexyl side chains. The α,ω-dihexylsexithiophene formed a large and well-ordered monolayer in which the molecule lay flatly on the Au(111) surface and was separated into two chiral domains. A detailed observation reveals that the admolecules were packed in one lamellae with their molecular axis aligned along the main axis of the Au(111) substrate with their hexyl chains deviated from <110> direction of the Au(111) substrate by 12 ± 0.5°. In contrast to the behavior in the three-dimensional bulk structure, flat-lying adsorption introduced molecular chirality: right- and left-handed molecules separate into domains of two different orientations, which are mirror symmetric with respect to the <121> direction of the Au(111) substrate. Details of the adlayer structure and the chiral self-assembly were discussed here.

Electron transfer and electrocatalytics of cytochrome c and horseradish peroxidase on DNA modified electrode.

A bio-interphase composed of DNA, cytochrome c (Cyt c) and horseradish peroxidase (HRP) was developed by layer-by-layer assembling Cyt c, DNA and Cyt c-HRP on biocompatible 11-mercaptoundecanoic acid--6-mercapto-1-hexanol modified gold electrode. The new bio-interphase was used as a model system to mimic the electron transfer and electrocatalytic performance of two proteins in living organisms. Results showed that the electron transfer rate at bi-protein bio-interphase was faster than those at the single protein bio-interphase, indicating a synergistic interaction between the two proteins occurred in the electron transfer. Moreover, the mixed proteins modified electrode exhibited good electrocatalytic response to reduction of hydrogen peroxide (H2O2) and oxygen (O2), suggesting that it could be used as a sensor for H2O2 and O2 detection. The properties of the bio-interphase, together with the bioelectrocatalytic activity, could make it useful in the development of bioelectronic devices, and investigation of electrochemistry of other heme proteins at functional interphase. It would also provide a new strategy for further study on the electron transfer of other multi-proteins in a bio-interphase and the development of biosensors.

Two-dimensional polymerization and reaction at the solid/liquid interface: scanning tunneling microscopy study.

The two-dimensional polymerization and reaction at the solid/liquid interface has caused considerable attention in recent years because of its fundamental importance and many potential applications. Scanning tunneling microscopy (STM) provides the possibility for the observation and manipulation of polymerization and reaction occurring at the solid/liquid interface at the atomic level. Two-dimensional polymerization and reaction could be induced by external stimuli, such as electrochemistry-induced, STM tip-induced, or light-induced. The polymerization at the solid/liquid interface is the focus of this review, including the mechanism of polymerization and characterization of structural and electrical properties of the resulting polymers. Finally, the outlooks for developments in this field are described.