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Dinitrosyl iron complexes (DNICs) are spontaneously and rapidly generated in cells. Their assembly requires nitric oxide (NO), biothiols, and nonheme iron, either labile iron or iron-sulfur clusters. Despite ubiquitous detection by electron paramagnetic resonance in NO-producing cells, the DNIC's chemical biology remains only partially understood. In this Forum Article, we address the reaction mechanisms for endogenous DNIC formation, with a focus on a labile iron pool as the iron source. The capability of DNICs to promote S-nitrosation is discussed in terms of S-nitrosothiol generation associated with the formation and chemical reactivity of DNICs. We also highlight how elucidation of the chemical reactivity and the dynamics of DNICs combined with the development of detection/quantification methods can provide further information regarding their participation in physiological and pathological processes.Bioinspired self-assembly has been explored with diverse synthetic scaffolds, among which amphiphiles are perhaps the most extensively studied systems. Classical surfactants or amphiphilic block copolymers, depending on the hydrophobic-hydrophilic balance, produce distinct nanostructures, which hold promise for applications ranging from biology to materials sciences. Nevertheless, their immiscibility-driven aggregation does not provide the opportunity to precisely regulate the internal order, morphology, or functional group display, which is highly desirable, especially in the context of biological applications.A new class of amphiphiles have emerged in the recent past in which the hydrophilic segment(s) is appended with a hydrophobic supramolecular-structure-directing-unit (SSDU), consisting of a π-conjugated chromophore and a H-bonding group. Self-recognition of the SSDU by attractive directional interactions governs the supramolecular assembly, which is fundamentally different than the repulsive solvent-immphiphiles, which by virtue of efficient and predictable functional group display, strongly influences the multivalent binding with different biological targets resulting in efficient enzyme inhibition, glycocluster effect, or antibacterial activity, depending on the nature of the functional group. By taking advantage of the electron accepting nature of the NDI, electron rich pyrene-containing amphiphiles can be costacked in alternating sequence, producing temperature and redox-responsive supramolecular polymers with NDI/pyrene stoichiometry-dependent morphology, lower critical solution temperature (LCST), functional group display, and antibacterial activity.Sr0.7Bi0.2TiO3 (SBT) is a promising pulse energy storage material due to minor hysteresis, but its low maximum polarization (Pmax) is bad for energy storage. K+-Bi3+ defect pairs were introduced into the A-site of SBT to obtain Sr0.35Bi0.35K0.25TiO3 (SBKT) with larger Pmax. Through first-principles calculations, we determined that the introduction of defect pairs destroys the paraelectric order phase and increases local polarization, resulting in more and larger polar nanoregion (PNR) formation. On this basis, doping NaNbO3 (NN) in A- and B-sites of SBKT increases the cationic disorder and ferroelectric destabilization, further destroying the long-range order structure and forming more PNRs with smaller sizes. This enhances relaxation and decreases remnant polarization, and the broadened dielectric peak enables 0.85SBKT-0.15NN to meet the X7R specification. Furthermore, the decreased grain size and oxygen vacancy, increased thermal conductivity, and weakened local electric field (simulated by COMSOL) increase the dielectric breakdown strength (BDS). As a result, 0.95SBKT-0.05NN exhibits a high energy storage density (W) of 2.45 J/cm3 with a high efficiency of 93.1%, a high pulsed discharge energy density of 2.1 J/cm3, and a high power density of 54.1 MW/cm3 at 220 kV/cm. The energy storage properties show excellent stability of temperature (-55 to 150 °C), frequency (10-500 Hz), and cycling (105 cycles). Notably, for the pulse charge-discharge properties, 0.95SBKT-0.05NN shows great fatigue resistance during 105 cycles under 25 and 150 °C, accompanied by excellent thermal stability. Moreover, the BDS and Pmax of 0.95SBKT-0.05NN sintered in O2 further enhance. A higher W of 2.92 J/cm3 with a high efficiency of 89% at 250 kV/cm is achieved. Therefore, 0.95SBKT-0.05NN shows great application potential for pulse energy storage. In this work, we provide a novel strategy and systematic in-depth study for improving the energy storage properties of SBT.The isolation and detection of rare circulating tumor cells (CTCs) from patient peripheral blood can help early diagnosis of cancer and evaluation of therapeutic outcomes. At present, most of the available strategies for enriching CTCs face serious problems with purity due to the nonspecific interactions between the capture medium and leukocytes. [https://www.selleckchem.com/products/sovilnesib.html Sovilnesib price] Inspired by the immune evasion ability of homologous red blood cells (RBCs), we modified the tumor-targeting molecule folic acid (FA) on the surface of RBCs by hydrophobic interactions. Under the treatment of polybrene, the charges on the surface of RBCs are neutralized, which reduces the mutual repulsion force. Furthermore, RBCs treated with polyethylene also have excellent deformability, thereby enabling engineered RBCs to form a dense bionic layer on the adhesive glass slide, which can greatly inhibit the nonspecific adhesion of leukocytes. The bionic layer can achieve high-purity enrichment of tumor cells in phosphate-buffered saline (PBS), and we can achieve high-activity release in plasma. The cell count showed over 80% capture efficiency and over 70% release rate, and the purity of CTCs obtained in the artificial blood sample after release was higher than 90%. The RBC bionic surface coating is notably cost-effective and highly applicable for CTC isolation in clinic practice, and thus provides new prospects for designing cell-material interfaces for advanced cell-based biomedical studies in the future.There is an imperative demand for real-time relative humidity (RH) discrimination with excellent sensitivity and robust operation stability over a broad RH range at room temperature (22 °C). Of diverse two-dimensional (2D) materials, p-type molybdenum disulfide (MoS2) as a typical gas-sensing candidate has been rarely harnessed for humidity detection due to tiny response and undesirable stability induced by the conversion from electron to proton conduction with increasing RH. To overcome these issues, MoS2-polyethylene oxide (PEO) inorganic-organic nanocomposites as the sensing layer were facilely prepared in this work. The results showed that the composition-optimized composite film sensor surpassed the isolated MoS2 counterpart in terms of repeatability, response, hysteresis, stability, and selectivity. Both DC-resistance and AC-impedance analyses unveiled different roles of MoS2 and PEO components within composites. MoS2 strengthened the film structure, while hydrophilic PEO enlarged the water-adsorption capacity and thus improved the response and detection reliability via water-triggered ionic conductivity.