A clathrin homolog encoded on human chromosome 22 (CHC22) displays distinct biochemistry, distribution and function compared with conventional clathrin heavy chain (CHC17), encoded on chromosome 17. CHC22 protein is upregulated during myoblast differentiation into myotubes and is expressed at high levels in muscle and at low levels in non-muscle cells, relative to CHC17. The trimeric CHC22 protein does not interact with clathrin heavy chain subunits nor bind significantly to clathrin light chains. CHC22 associates with the AP1 and AP3 adaptor complexes but not with AP2. In non-muscle cells, CHC22 localizes to perinuclear vesicular structures, the majority of which are not clathrin coated. Treatments that disrupt the actin-myosin cytoskeleton or affect sorting in the trans-Golgi network (TGN) cause CHC22 redistribution. Overexpression of a subdomain of CHC22 induces altered distribution of TGN markers. Together these results implicate CHC22 in TGN membrane traffic involving the cytoskeleton.
A high‐surface‐area, highly crystalline boron nitride aerogel synthesized with nonhazardous reactants has been loaded with crystalline platinum nanoparticles to form a novel nanomaterial that exhibits many advantages for use in a catalytic gas sensing application. The platinum nanoparticle‐loaded boron nitride aerogel integrated onto a microheater platform allows for calorimetric propane detection. The boron nitride aerogel exhibits thermal stability up to 900 °C and supports disperse platinum nanoparticles, with no sintering observed after 24 h of high‐temperature testing. The high thermal conductivity and low density of the boron nitride aerogel result in an order of magnitude faster response and recovery times (<2 s) than reported on alumina support and allow for 10% duty cycling of the microheater with no loss in sensitivity. The resulting 1.5 mW sensor power consumption is two orders of magnitude less than commercially available catalytic gas sensors and unlocks the potential for wireless, battery‐powered catalytic gas sensing.
Surface oxidation states of transition (Fe and Co) and noble (Pd and Pt) metals were tailored by controlled exposure to O2 plasmas, thereby enabling their removal by specific organic chemistries. Of all organic chemistries studied, formic acid was found to be the most effective in selectively removing the metal oxide layer in both the solution and vapor phase. The etch rates of Fe, Co, Pd, and Pt films, through an alternating plasma oxidation and formic acid vapor reaction process, were determined to be 4.2, 2.8, 1.2, and 0.5 nm/cycle, respectively. Oxidation by atomic oxygen was an isotropic process, leading to an isotropic etch profile by organic vapor. Oxidation by low energy and directional oxygen ions was an anisotropic process and thus results in an anisotropic etch profile by organic vapor. This is successfully demonstrated in the patterning of Co with a high selectivity over the TiN hardmask, while preserving the desired static magnetic characteristic of Co.
An ion beam-assisted organic vapor etch process is demonstrated for patterning magnetic metal elements for potential applications in magnetoresistive random access memory devices. A thermodynamic analysis was performed to evaluate the feasibility of a chemical etch process, leading to the selection of acetylacetone (acac) and hexafluoroacetylacetone (hfac) chemistries. First, etching of cobalt and iron in acac and hfac solutions was studied, and it was determined that acac etches Co preferentially over Fe with a Co:Fe selectivity of ∼4, while hfac etches Fe preferentially over Co with an Fe:Co selectivity of ∼40. This motivates the use of acac and hfac to etch Co and Fe, respectively, but the etch rate was, in the gas phase, too small to be considered a viable process. An argon ion beam was employed in between organic vapor exposures and resulted in significant enhancement in the etch rates, suggesting an ion-enhanced chemical etching process is viable for the patterning of these magnetic metal elements.
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