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Cytochrome P450 2D6 (CYP2D6) is a key enzyme that mediates the metabolism of various drugs and endogenous substances in humans. However, its biological role in drug‐drug interactions especially mechanism‐based inactivation (MBI), and various diseases remains poorly understood, owing to the lack of molecular tools suitable for selectively monitoring CYP2D6 in complex biological systems. Herein, using a tailored molecular strategy, we developed a fluorescent probe BDPM for CYP2D6. BDPM exhibits excellent specificity and imaging capability for CYP2D6, making it suitable for the real‐time monitoring of endogenous CYP2D6 activity in living bio‐samples. Therefore, our tailored strategy proved useful for constructing the highly selective and enzyme‐activated fluorescent probes. BDPM as a molecular tool to explore the critical roles of CYP2D6 in the pathogenesis of diseases, high‐throughput screening of inhibitors and intensive investigation of CYP2D6‐induced MBI in natural systems. [ABSTRACT FROM AUTHOR]

Flexible wearable strain sensors have received extensive attention in human–computer interaction, soft robotics, and human health monitoring. Despite significant efforts in developing stretchable electronic materials and structures, developing flexible strain sensors with stable interfaces and low hysteresis remains a challenge. Herein, Ti3C2Tx MXene/AgNWs/liquid metal strain sensors (MAL strain sensor) with self‐healing function are developed by exploiting the strong interactions between Ti3C2Tx MXene/AgNWs/LM and the disulfide and hydrogen bonds inside the self‐healing poly(dimethylsiloxane) elastomers. AgNWs lap the Ti3C2Tx MXene sheets, and the LM acts as a bridge to increase the lap between Ti3C2Tx MXene and AgNWs, thereby improving the interface interaction between them and reducing hysteresis. The MAL strain sensor can simultaneously achieve high sensitivity (gauge factor for up to 3.22), high linearity (R2 = 0.98157), a wide range of detection (e.g., 1%–300%), a fast response time (145 ms), excellent repeatability, and stability.In addition, the MAL strain sensor before and after self‐healing is combined with a small fish and an electrothermally driven soft robot, respectively, allowing real‐time monitoring of the swinging tail of the small fish and the crawling of the soft robot by resistance changes. [ABSTRACT FROM AUTHOR]

Developing multifunctional electronic fabrics with sensing capabilities, electromagnetic interference (EMI) shielding, and Joule heating performance holds great significance for health monitoring and medical protection. However, most fabrics struggle to combine multiple functions and optimize them simultaneously. For example, achieving both high sensitivity and a wide detection range in sensing devices remains a challenge. In this paper, we present a multidimensional composite structure comprising MXene Ti3C2Tx nano lamellar, self-assembled lotus leaf-like MXene/EGaIn and carbon nanotubes (CNTs) assembled on the surface of thermoplastic polyurethane to create a multifunctional MXene EGaIn/MXene CNT fabric (MEMC fabric). The multidimensional materials form a stable conductive network under tension. As a strain sensor, the MEMC fabric exhibits a large sensing range (0–360%) and ultra-high sensitivity (GF ∼ 114,700), making it suitable for artificial eardrum research. Additionally, MEMC demonstrates excellent EMI shielding effect (∼73 dB) and maintains good EMI shielding performance under tensile conditions. The fabric also showcases outstanding Joule heating performance (low voltage drive ∼2 V, fast heating time ∼13 s, and high heating stability ∼4000 s). This paper also demonstrates the multifunctional combination of MEMC fabrics, achieving simultaneous sensing, EMI shielding, and Joule heating functions under stretching. This work offers a forward-looking approach for constructing multifunctional composite fabrics, and the resulting MEMC composite materials hold potential applications in portable electronic devices and defense industries. [ABSTRACT FROM AUTHOR]

Ti3C2Tx MXene has a high specific surface area and high conductivity, and can be used in the field of humidity sensing. By controlling the surface termination and microstructure of the material, it is expected to improve the humidity sensing performance of Ti3C2Tx MXene. In this paper, we report a method of electrolytic intercalation treatment of Ti3C2Tx MXene in NaOH solution. Theoretical and experimental results show that this method can remove the original F terminations from the surface of Ti3C2Tx MXene and form a large number of OH and O terminations. The partial oxidation of the surface and the replacement of terminations and the insertion of Na+ lead to the change of the Ti3C2Tx MXene layer morphology from flat to curly and significantly improve the hydrophilicity and resistance. The curly flake structure constructs a fast channel for the entry and exit of water molecules which improves the hydration/dehydration efficiency of the material; the enhanced hydrophilicity of the material sharply reduces the resistance of the material after moisture absorption, which significantly improves the responsiveness of Ti3C2Tx MXene to humidity. The curly flake Ti3C2Tx MXene humidity sensor has an ultra-high sensitivity of S = 1.2 × 105 (two orders of magnitude higher than that of the reported humidity sensor based on MXene), with a fast response rate (2 s), good repeatability and stability (4 weeks), and it can be used for the analysis of human respiration rate, and also for non-contact sensing detection of the human body and environmental humidity detection. [ABSTRACT FROM AUTHOR]

Mechanism‐based inactivation (MBI) can mediate adverse reactions and hepatotoxicity from drugs, which is a result of their conversion into highly reactive metabolites catalyzed by enzymes such as cytochrome P450 3A (CYP3A). In the present research, we optimized the key interaction domain of the fluorophore with the target protein to develop a two‐photon fluorescent probe for CYP3A that is involved in the metabolism of more than half of all clinical drugs. The developed BN‐1 probe exhibited appropriate selectivity and sensitivity for the semi‐quantitative detection and imaging of endogenous CYP3A activity in various living systems, thereby providing a high‐throughput screening system enabling evaluation of MBI‐associated hepatotoxicity by CYP3A. Using BN‐1 as a fluorescent molecular tool facilitates the efficient discovery and characterization of CYP3A‐induced MBI in natural systems. [ABSTRACT FROM AUTHOR]

The bone marrow (BM) niches are the complex microenvironments that surround cells, providing various external stimuli to regulate a range of haematopoietic stem cell (HSC) behaviours. Recently, it has been proposed that the fate decision of HSCs is often correlated with significantly altered biophysical signals of BM niches. To thoroughly elucidate the effect of mechanical microenvironments on cell fates, we constructed 2D and 3D cell culture hydrogels using polyacrylamide to replicate the mechanical properties of heterogeneous sub‐niches, including the inherent rigidity of marrow adipose tissue (2 kPa), perivascular tissue (8 kPa) and endosteum region (35 kPa) in BM. Our observations suggest that HSCs can respond to the mechanical heterogeneity of the BM microenvironment, exhibiting diversity in cell mechanics, haematopoietic pool maintenance and differentiated lineages. Hydrogels with higher stiffness promote the preservation of long‐term repopulating HSCs (LT‐HSCs), while those with lower stiffness support multi‐potent progenitors (MPPs) viability in vitro. Furthermore, we established a comprehensive transcriptional profile of haematopoietic subpopulations to reflect the multipotency of haematopoietic stem and progenitor cells (HSPCs) that are modulated by niche‐like stiffness. Our findings demonstrate that HSPCs exhibit completely distinct downstream differentiated preferences within hydrogel systems of varying stiffness. This highlights the crucial role of tissue‐specific mechanical properties in HSC lineage decisions, which may provide innovative solutions to clinical challenges. [ABSTRACT FROM AUTHOR]

The increasing pressure and unhealthy lifestyle are gradually eroding the physical and mental health of modern people. As a key hormone responsible for maintaining the normal functioning of human systems, cortisol plays a vital role in regulating physiological activities. Moreover, cortisol can serve as a marker for monitoring psychological stress. The development of cortisol detection sensors carries immense potential, as they not only facilitate timely adjustments and treatments by detecting abnormal physiological indicators but also provide comprehensive data for conducting research on the correlation between cortisol and several potential diseases. Here, we report a molecularly imprinted polymer (MIP) electrochemical biosensor that utilizes a porous composite (MXG) modified electrode. MXG composite is prepared by combining Ti 3 C 2 T x -MXene sheets and graphene (Gr). MXG composite material with high conductive properties and large electroactive surface area promotes the charge transfer capability of the electrode surface, expands the effective surface area of the sensor, and increases the content of cortisol-imprinted cavities on the electrode, thereby improving the sensing ability of the sensor. By optimizing the preparation process, the prepared sensor has an ultralow lower limit of detection of 0.4 fM, a wide detection range of 1 fM-10 μM, and good specificity for steroid hormones and interfering substances with similar cortisol structure. The ability of the sensor to detect cortisol in saliva was also confirmed experimentally. This highly sensitive and selective cortisol sensor is expected to be widely used in the fields of physiological and psychological care.