Camachowebster6899

Perfluoroalkyl substances (PFASs) persist and are ubiquitous in the environment. The origins of PFAS toxicity and how they specifically affect the functions of proteins remain unclear. Herein, we report that PFASs can strongly inhibit the activity of human carbonic anhydrases (hCAs), which are ubiquitous enzymes that catalyze the hydration of CO2, are abundant in the blood and organs of mammals, and involved in pH regulation, ion homeostasis, and biosynthesis. The interactions between PFASs and hCAs were investigated using stopped-flow kinetic enzyme-inhibition measurements, native mass spectrometry (MS), and ligand-docking simulations. Narrow-bore emitters in native MS with inner diameters of ∼300 nm were used to directly and simultaneously measure the dissociation constants of 11 PFASs to an enzyme, which was not possible using conventional emitters. The data from native MS and stopped-flow measurements were in excellent agreement. selleckchem Of 15 PFASs investigated, eight can inhibit at least one of four hCA isozymes (I, II, IX, and XII) with submicromolar inhibition constants, including perfluorooctanoic acid, perfluorooctanesulfonamide, and perfluorooctanesulfonic acid. Some PFASs, including those with both short and long perfluoromethylene chains, can effectively inhibit at least one hCA isozyme with low nanomolar inhibition constants.Developing effective and nonprecious electrocatalysts is an indispensable requirement for boosting the efficiency of water splitting to obtain clean and sustainable fuels. Herein, we reported a feasible strategy for preparing a trimetallic (NiCoFe) superior electrocatalyst with novel open-cage/3D frame-like structure for oxygen evolution reaction (OER). It is prepared by consequence thermal treatments of CoFe Prussian blue analog frame/cage-like structure under Argon (CoFeA-TT) atmosphere, and then electrodeposition of Nickel-Cobalt Sulfide nanosheets as shell layer on it. The electrochemical measurements demonstrated that the deposition of NiCoS on CoFeA-TT (NiCo-S@CoFeA-TT) has the best catalytic performance and can drive the benchmark current density of 10 mA cm-2 at a low overpotential of 268 mV with a Tafel slope of 62 mV dec-1 and an excellent long term catalytic stability in alkaline medium. Its outstanding electrocatalytic performances are benefited from frame/cage-like structures, highly exposed active sites, accelerated mass and electron transport, and synergistic effect of multiple hybrid components. The NiCo-S@CoFeA-TT showed to act better than most advanced nonprecious catalysts and noble commercial RuO2 catalyst. This work exhibited an effective and efficient approach to design three-dimensional porous architecture catalysts for the energy-relevant electro-catalysis reaction.Developing high-efficiency and cost-effective electrocatalysts for the oxygen evolution reaction (OER) is crucial for various energy conversion systems. Herein, N/S co-doped C encapsulated hollow NiCo2O4/NiO hexagonal rods (HNHR@N/S-C) as the electrocatalysts for OER have been successfully prepared with rational control of structure and composition. Experimental and theoretical results have highlighted that the NiCo2O4/NiO heterojunction in the obtained electrocatalyst can provide abundant active Ni and Co sites for the OER, leading to the highly enhanced OER performance. Moreover, attributed to the hierarchical hollow structure, which can provide a large surface area, and the improved electric conductivity with a coating of the N/S co-doped carbon layer, which can facilitate charge transport during the catalytic processes, a remarkable OER activity over HNHR@N/S-C with a low overpotential (η) of 285 mV (at j = 10 mA cm-2) and a Tafel slope of 53.0 mV decade-1 has been achieved, which is comparable to that of the noble metal catalyst IrO2. Because of the protection of the N/S doped C layer coating, HNHR@N/S-C can also maintain the current density of 10 mA cm-2 for at least 12 h in alkaline media without obvious losses of activity.Photodynamic therapy (PDT) possesses two pathways depending on the type of high-toxicity reactive oxygen species (ROS), superoxide anion radical (O2·-) and hydroxyl radical (·OH) generated through Type I and singlet oxygen (1O2) generated through Type II, inducing cancer cell apoptosis. However, the low efficiency of ROS generation and poor biocompatibility are the limitations of the traditional photosensitizers for PDT. Herein, inspired by photochemical reactions of titanium dioxide and porphyrin-based metal-organic frameworks, we developed a nanoplatform by covering ultrasmall titanium dioxide nanoparticles on a heterodimer made up of upconversion nanoparticles and metal-organic frameworks, realizing a multimode PDT through Type I and Type II mechanisms. Once irradiated by a near-infrared light, upconversion nanoparticles could generate ultraviolet and visible lights, which were not only able to stimulate different photochemical reactions of titanium dioxide and porphyrin but also accomplish deep penetration photodynamic therapy. Our photosensitive agent exhibited good biocompatibility and an effective multimode PDT performance, which could meet the needs of different situations of photodynamic therapy in the future.Three new quaternary Zintl phases with the "9-4-9" formula, Ae9Mn4-xAlxSb9 (Ae = Ca, Yb, Eu), have been synthesized using Pb as the metal flux, and their crystal structures have been established by single-crystal X-ray diffraction. Both Ca9Mn2.91(4)Al1.09Sb9 and Yb9Mn3.59(6)Al0.41Sb9 are isostructural with Ca9Mn4Bi9, and they crystallize in the orthorhombic space group Pbam with unit cell dimensions of a = 12.4571(8), 12.2884(16) Å, b = 22.1352(16), 22.024(3) Å, and c = 4.6012(3), 4.6187(6) Å, respectively. Their anionic structures can be viewed as infinite ribbons based on corner-shared tetrahedrons. Also, Eu9Mn2.87(4)Al1.13Sb9 has the space group Cmca and a = 9.4883(7) Å, b = 23.6895(18) Å, and c = 24.4845(19) Å. The structural relationships between Ca9Mn2.91(4)Al1.09Sb9 and Eu9Mn2.87(4)Al1.13Sb9 are compared and discussed as well. The successful Al3+ substitution provides additional electrons to the compounds to achieve structural stability. Magnetic susceptibility and electrical resistivity measurements, performed on single crystals of Eu9Mn2.