Gene/Protein Disease Symptom Drug Enzyme Compound
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Via the activation treatment of carbonized almond shells with HNO3 and KOH, activated microporous carbon (AMC-3 and AMC-2) was successfully synthesized. These two AMC electrodes demonstrate remarkable electrochemical behaviors such as high rate capability, high specific capacitance, and excellent cycle stability when serving as electrodes for supercapacitors. More importantly, through the use of a Zn-Ni-Co ternary oxide (ZNCO) positive electrode and the AMC negative electrode, asymmetric supercapacitors (ASC) were assembled that deliver superior energy density (53.3 Wh kg(-1) at a power density of 1126.1 W kg(-1) for ASC-2 and 53.6 Wh kg(-1) at a power density of 1124.5 W kg(-1) for ASC-3) and excellent stability (82.7% and 83.4% specific capacitance retention for ZNCO//AMC ASC-2 and ZNCO//AMC ASC-3, respectively, after 5000 cycles). Through these two methods, low-cost, renewable, and environmentally friendly electrode materials can be provided for high energy density supercapacitors.
ACS Appl Mater Interfaces 2016 Jun 22
PMID:Activated Microporous Carbon Derived from Almond Shells for High Energy Density Asymmetric Supercapacitors. 2725 80

Surface-imprinted nanoparticles with double recognition (DM-MIPs) are fabricated onto halloysite nanotubes (HNTs) for highly specific separation of natural flavone luteolin (LTL) under neutral condition. Specifically, a two-step strategy via consecutive surface-initiated atom transfer radical polymerization (SI-ATRP) is employed to introduce inherent recognition of molecular imprinting and reversible covalent affinity of boronic acid ligands and immobilized Zn2+ into DM-MIPs. First, Zn2+-immobilized poly(vinyl imidazole) (PVLD) shell based on the HNTs via the first SI-ATRP is prepared to capture LTL by metal chelating. Then HNTs-supported surface imprinted nanoparticles are prepared using low pKa boronic acid monomer 4-(2-acrylamidoethylcarbamoyl)-3-fluorophenylboronic acid (AMC-FPBA) via the second SI-ATRP. Taking advantage of low apparent pKa of AMC-FPBA and large high-affinity binding site density, DM-MIPs possess a promising binding with cis-diol-containing LTL under neutral condition. In static adsorption, DM-MIPs show large LTL loading amount (83.42 mg g-1), fast capture kinetics, remarkable selectivity, and excellent recyclability at pH = 7.0. More importantly, by reducing the pH to 4.0, the loaded TLL can be simply released. As a proof of this concept, a commercially available LTL with 85% purity can be easily enriched and further purified, and the product exhibits the similar antibacterial performance with standard substance.
ACS Appl Mater Interfaces 2017 Sep 27
PMID:Two Are Better than One: Halloysite Nanotubes-Supported Surface Imprinted Nanoparticles Using Synergy of Metal Chelating and Low pKa Boronic Acid Monomers for Highly Specific Luteolin Binding under Neutral Condition. 2888 1

Caspase-1 is a key player in pyroptosis and inflammation. Caspase-1 inhibition is found to be beneficial to various diseases. Coumarin-originated natural products have an anti-inflammation function, but their direct inhibition effect to caspase-1 remains unexplored. To evaluate their interactions, the widely used commercial coumarin-based probe (Ac-YVAD-AMC) is not suitable, as the background signal from coumarin-originated natural products could interfere with the screening results. Therefore, fluorescent probes using a large Stokes shift could help solve this problem. In this work, we chose the fluorophore of tetraphenylethylene-thiophene (TPETH) with aggregation-induced emission characteristics and a large Stokes shift of about 200 nm to develop a molecular probe. Bioconjugation between TPETH and hydrophilic peptides (DDYVADC) through a thiol-ene reaction generated a light-up probe, C1-P3. The probe has little background signal in aqueous media and exerts a fluorescent turn-on effect in the presence of caspase-1. Moreover, when evaluating the inhibition potency of coumarin-originated natural products, the new probe could generate a true and objective result but not for the commercial probe (Ac-YVAD-AMC), which is evidenced by HPLC analysis. The quick light-up response and accurate screening results make C1-P3 very useful in fundamental study and inhibitior screening toward caspase-1.
ACS Appl Mater Interfaces 2018 Apr 18
PMID:Caspase-1 Specific Light-Up Probe with Aggregation-Induced Emission Characteristics for Inhibitor Screening of Coumarin-Originated Natural Products. 2932 74

Proteases within the C1B hydrolase family are encoded by many organisms. We subjected a putative C1B-like cysteine protease secreted by the human gut commensal Parabacteroides distasonis to mass spectrometry-based substrate profiling to find preferred peptide substrates. The P. distasonis protease, which we termed Pd_dinase, has a sequential diaminopeptidase activity with strong specificity for N-terminal glycine residues. Using the substrate sequence information, we verified the importance of the P2 glycine residue with a panel of fluorogenic substrates and calculated kcat and KM for the dipeptide glycine-arginine-AMC. A potent and irreversible dipeptide inhibitor with a C-terminal acyloxymethyl ketone warhead, glycine-arginine- AOMK, was then synthesized and demonstrated that the Pd_dinase active site requires a free N-terminal amine for potent and rapid inhibition. We next determined the homohexameric Pd_dinase structure in complex with glycine-arginine- AOMK and uncovered unexpected active site features that govern the strict substrate preferences and differentiate this protease from members of the C1B and broader papain-like C1 protease families. We finally showed that Pd_dinase hydrolyzes several human antimicrobial peptides and therefore posit that this P. distasonis enzyme may be secreted into the extracellular milieu to assist in gut colonization by inactivation of host antimicrobial peptides.
ACS Chem Biol 2018 09 21
PMID:A Commensal Dipeptidyl Aminopeptidase with Specificity for N-Terminal Glycine Degrades Human-Produced Antimicrobial Peptides in Vitro. 3008 57

The effects of alkaline-earth metal cation (AMC; Mg2+, Ca2+, Sr2+, and Ba2+) substitution on the photoelectrochemical properties of phase-pure LaFeO3 (LFO) thin-films are elucidated by X-ray photoemission spectroscopy (XPS), X-ray diffraction (XRD), diffuse reflectance, and electrochemical impedance spectroscopy (EIS). XRD confirms the formation of single-phase cubic LFO thin films with a rather complex dependence on the nature of the AMC and extent of substitution. Interestingly, subtle trends in lattice constant variations observed in XRD are closely correlated with shifts in the binding energies of Fe 2p3/2 and O 1s orbitals associated with the perovskite lattice. We establish a scaling factor between these two photoemission peaks, unveiling key correlation between Fe oxidation state and Fe-O covalency. Diffuse reflectance shows that optical transitions are little affected by AMC substitution below 10%, which are dominated by a direct bandgap transition close to 2.72 eV. Differential capacitance data obtained from EIS confirm the p-type characteristic of pristine LFO thin-films, revealing the presence of sub-bandgap electronic state (A-states) close to the valence band edge. The density of A-states is decreased upon AMC substitution, while the overall capacitance increases (increase in dopant level) and the apparent flat-band potential shifts toward more positive potentials. This behavior is consistent with the change in the valence band photoemission edge. In addition, capacitance data of cation-substituted films show the emergence of deeper states centered around 0.6 eV above the valence band edge (B-states). Photoelectrochemical responses toward the hydrogen evolution and oxygen reduction reactions in alkaline solutions show a complex dependence on alkaline-earth metal incorporation, reaching incident-photon-to-current conversion efficiency close to 20% in oxygen saturated solutions. We rationalize the photoresponses of the LFO films in terms of the effect sub-bandgap states on majority carrier mobility, charge transfer, and recombination kinetics.
ACS Appl Mater Interfaces 2020 Jul 15
PMID:Promoting Active Electronic States in LaFeO3 Thin-Films Photocathodes via Alkaline-Earth Metal Substitution. 3253 32

A number of techniques, including conductivity, surface tension, dynamic light scattering, transmission electron microscopy, and 1H nuclear magnetic resonance (1H NMR), Fourier transform infrared (FT-IR), and 1H-1H 2D nuclear Overhauser effect spectroscopy (1H-1H 2D NOESY), have been used to investigate the effect of amide bonds on the interfacial and assembly properties of a cationic surfactant, N-anilinoformylmethyl-N-cetyl-N,N-dimethyl ammonium chloride (AMC-C 16 ), in aqueous solutions. The adsorption of AMC-C 16 has been found to be much better than that of the conventional cationic surfactant, benzyl cetyldimethylammonium chloride (BAC-16) at the air/water interface and in solution. The surface tension measurements show the presence of two critical aggregation concentrations (CAC1 and CAC2) for AMC-C 16 . The presence of a strong intermolecular hydrogen bond of AMC-C 16 was confirmed by 1H NMR and FT-TR. The molecular interactions of AMC-C 16 were detected by 1H-1H 2D NOESY. The results show that the rigid group (phenyl) of AMC-C 16 was partially overlapped with its alkyl chain in aqueous solution, and the possible aggregation behavior for AMC-C 16 was proposed. The effects of an inorganic salt (NaCl) and an organic salt (C6H5COONa) to the aggregates of AMC-C 16 have been discussed.
ACS Omega 2020 Jul 21
PMID:Study on the Surface Properties and Aggregation Behavior of Quaternary Ammonium Surfactants with Amide Bonds. 3271 89