Strausszimmermann2336

Metal-organic frameworks (MOFs)-supported noble metal nanoparticles (NMNPs) catalysts attract increasing attention due to their high durability and efficiency in catalytic reactions. In this work, Pt nanoparticles are inserted at the designated location inside MIL-100(Fe) to investigate the location-effect of NMNPs inside MOFs on the catalytic reaction. The comparison test on the reduction of p-nitrophenol suggests that the location of the Pt nanoparticles inside MIL-100(Fe) largely influences the catalytic performance and the Pt nanoparticles inside MIL-100(Fe) locate closer to the outer surface of the MIL-100(Fe), providing higher catalytic efficiency. Possible reasons are concluded as the location of the Pt nanoparticles inside MIL-100(Fe) dominates the reactants transport pathway and the loading amount of Pt nanoparticles.Lectins are omnipresent carbohydrate binding proteins that are involved in a multitude of biological processes. Unearthing their binding properties is a powerful tool toward the understanding and modification of their functions in biological applications. Herein, we present the synthesis of glycopolymers with a brush architecture via a "grafting from" methodology. The use of a versatile 2-oxazoline inimer was demonstrated to open avenues for a wide range of 2-oxazoline/acrylamide bottle brush polymers utilizing aqueous Cu-mediated reversible deactivation radical polymerization (Cu-RDRP). The polymers in the obtained library were assessed for their thermal properties in aqueous solution and their binding toward the C-type animal lectins dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN) and mannose-binding lectin (MBL) via surface plasmon resonance spectrometry. The encapsulation properties of a hydrophobic drug-mimicking compound demonstrated the potential use of glyco brush copolymers in biological applications.Chemically modified antigen-binding proteins are widely applied for their targeting abilities in the fields of biotechnology, medicine, and diagnostics. However, the production of site-selectively modified proteins remains a challenge. Here, we have designed a chemical probe for the introduction of a reactive aldehyde on nanobodies by metal-complex-guided conjugation. The probe design allows for purification of the conjugates, and the aldehyde constitutes an efficient handle for further modification of the nanobodies. RI-1 price In vitro experiments confirmed the binding activity and selectivity of fluorescent conjugates toward the native antigen. Furthermore, the modification strategy allowed for production of a nanobody-drug conjugate that was active in vitro.Quartz fiber, a widely used reinforcer with high tensile strength and excellent heat resistance, can have more attractive electrical applications such as electromagnetic interference shielding, static dissipation, and strain sensing if it becomes conductive. Many attempts have been made to increase the electrical conductivity of quartz fiber by surface coating of conductive polymers or plating of metal films, but suffers from sacrificing flexibility and causing heavy metal pollution. Here we designed and massively produced a hybrid structure of graphene quartz fiber (GQF) by a forced-flow chemical vapor deposition (CVD) method, which combines the excellent conductivity of graphene and the extraordinary properties of quartz fiber. The as-fabricated flexible GQF exhibited high sensitivity, fast response ( less then 0.5 s) and good durability (∼5000 cycles) to organic solvent vapor, suitable as a real-time biomimetic gas sensor. Furthermore, the massively produced GQFs can be knitted into meter-scale fabrics with tunable conductivity (sheet resistances of 0.2-10 kΩ/sq) and superior electrothermal conversion efficiency (up to 980 °C within a few seconds at 24 V), thus propelling its promising application in industrial electric heaters. We expect this hybrid GQF material will greatly expand the applications of traditional quartz fiber into an infusive multifunctional regime.The efficient discrimination of oxidizing anions is of considerable importance in environmental monitoring. Here, for the first time, we have developed a simple and fast colorimetric sensor array for detection and identification of oxidizing anions, which takes advantage of the etching of the Ag shell of two core-shell Au@Ag nanoparticles (Au@Ag nanospheres (Au@Ag NPs) and Au@Ag nanocubes (Au@Ag NCs)) by oxidizing anions. The differential etching ability of various oxidizing anions to the Ag shell of the two Au@Ag nanoparticles resulted in different absorbance and color change of the nanoparticles. Thus, employing Au@Ag NPs and Au@Ag NCs as the array's receptors and the indicators, six oxidizing anions (i.e., BrO3-, Cr2O72-, ClO4-, IO3-, IO4-, and MnO4-) down to 10 nM could be identified from each other by their own colorimetric response patterns. Moreover, the complex mixtures of oxidizing anions could be well discriminated. Most importantly, the sensor array was successfully applied to the discrimination of oxidizing anions in river water and tap water samples.The bacterial toxin RelE cleaves mRNA in the ribosomal A site. Although it shares a global fold with other microbial RNases, the active site contains several positively charged residues instead of histidines and glutamates that are typical of ribonucleases. The pH dependences of wild-type and mutant RelE indicate it uses general acid-base catalysis, but either the general acid (proposed to be R81) or the general base must have a substantially downshifted pKa. However, which group is shifted cannot be determined using available structural and biochemical data. Here, we use a phosphorothiolate at the scissile phosphate to remove the need for a general acid. We show this modification rescues nearly all of the defect of the R81A mutation, supporting R81 as the general acid. We also find that the observed pKa of the general base is dependent on the charge of the side chain at position 81. This indicates that positive charge in the active site contributes to a general base pKa downshifted by more than 5 units. Although this modestly reduces the effectiveness of general acid-base catalysis, it is strongly supplemented by the role of the positive charge in stabilizing the transition state for cleavage.