SiO2 bridged AlN/methylphenyl silicone resin composite with integrated superior insulating property, high-temperature resistance, and high thermal conductivity.

A high-temperature-resistance insulating layer with high thermal conductivity is the key component for fabricating the instant metal-based electric heating tube. However, it is still a challenge for materials to possess excellent high-temperature resistance, superior insulating property, and high thermal conductivity at the same time. Here, a novel SiO2 bridged AlN/MSR composite based on methylphenyl silicone resin (MSR) and AlN filler was reported. MSR with a high thermal decomposition temperature of 452.0 °C and a high withstand voltage of 5.6 kV was first synthesized by adjusting the contents of alkyl and phenyl groups. The superior high-temperature resistant insulating property is 3.7 and 2.4 times higher than the national standard requirement of 1.5 kV and commercial silicone resin, respectively. The hydrogen bonds formed between SiO2, AlN, and MSR and the electrostatic adsorption between SiO2 and AlN can remarkably improve the uniform dispersion of AlN in MSR and thus enhance the insulating property, thermal conductivity, and thermal stability. With the addition of 2 wt% SiO2 and 50 wt% AlN, the SiO2-AlN/MSR composite exhibits an extremely high withstand voltage of 7.3 kV, a high thermal conductivity of 0.553 W·m-1·K-1, and an enhanced decomposition temperature of 475 °C. The superior insulating property and thermal conductivity are 4.9 and 1.3 times higher than the national standard requirement and pure MSR, respectively. This novel composite shows great potential for application in the fields requiring integrated superior insulating property, high-temperature resistance, and high thermal conductivity.

Enhancing Structure Stability by Mg/Cr Co-Doped for High-Voltage Sodium-Ion Batteries.

P2-Na2/3Ni1/3Mn2/3O2 cathode materials have garnered significant attention due to their high cationic and anionic redox capacity under high voltage. However, the challenge of structural instability caused by lattice oxygen evolution and P2-O2 phase transition during deep charging persists. A breakthrough is achieved through a simple one-step synthesis of Cr, Mg co-doped P2-NaNMCM, resulting in a bi-functional improvement effect. P2-NaNMCM-0.01 exhibits an impressive capacity retention rate of 82% after 100 cycles at 1 C. In situ X-ray diffraction analysis shows that the "pillar effect" of Mg mitigates the weakening of the electrostatic shielding and effectively suppresses the phase transition of P2-O2 during the charging and discharging process. This successfully averts serious volume expansion linked to the phase transition, as well as enhances the Na+ migration. Simultaneously, in situ Raman spectroscopy and ex situ X-ray photoelectron spectroscopy tests demonstrate that the strong oxygen affinity of Cr forms a robust TM─O bond, effectively restraining lattice oxygen evolution during deep charging. This study pioneers a novel approach to designing and optimizing layered oxide cathode materials for sodium-ion batteries, promising high operating voltage and energy density.

Insights into the Conductive Network of Electrochemical Exfoliation with Graphite Powder as Starting Raw Material for Graphene Production.

Electrochemical exfoliation starting with graphite powder as the raw material for graphene production shows superiority in cost effectiveness over the popular bulk graphite. However, the crucial conductive network inside the graphite powder electrode along with its formation and influence mechanisms remains blank. Here, an adjustable-pressure graphite powder electrode with a sandwich structure was designed for this. Appropriate encapsulation pressure is necessary and conducive to constructing a continuous and stable conductive network, but overloaded encapsulation pressure is detrimental to the exfoliation and graphene quality. With an initial encapsulation pressure (IEP) of 4 kPa, the graphite powders expand rapidly to a final stable expansion pressure of 49 kPa with a final graphene yield of 46.3%, where 84% of the graphene sheets are less than 4 layers with ID/IG values between 0.22 and 1.24. Increasing the IEP to 52 kPa, the expansion pressure increases to 73 kPa, but the graphene yield decreases to 39.3% with a worse graphene quality including higher layers and ID/IG values of 1.68-2.13. In addition, small-size graphite powders are not suitable for the electrochemical exfoliation. With the particle size decreasing from 50 to 325 mesh, the graphene yield decreases almost linearly from 46.3% to 5.5%. Conductive network and electrolyte migration synergize and constrain each other, codetermining the electrochemical exfoliation. Within an encapsulated structure, the electrochemical exfoliation of the graphite powder electrode proceeds from the outside to the inside. The insights revealed here will provide direction for further development of electrochemical exfoliation of graphite powder to produce graphene.

Constructing three-dimensional N-doped carbon coating silicon/iron silicide nanoparticles cross-linked by carbon nanotubes as advanced anode materials for lithium-ion batteries.

Silicon (Si), have been considered as promising anode material for lithium-ion batteries (LIBs), due to its high theoretical specific capacity of 4200 mAh g-1. However, the poor electrical conductivity and large volume change during lithiation/delithiation process, resulting in poor cycling stability, and seriously hindered the practical application in LIBs. Herein, a multiple Si/FexSiy@NC/CNTs composite is synthesized and investigated as advanced anode materials for LIBs via a simple one-step method. Such multiple Si/FexSiy@NC/CNTs composite has several merits including the FexSiy can not only accommodate the huge volume change of Si nanoparticles, but also enhance the conductivity upon discharge/charge process. Furthermore, the in-situ growth CNTs may help establish a long-range conductivity, and the Nitrogen-doped carbon (NC) layer can further improve the conductivity of Si, as well as inhibit the direct contract between electrolyte and Si during cycling process. Accordingly, the Si/FexSiy@NC/CNTs-1 exhibits excellent cycling stability (a high capacity of 994.4 mAh g-1 is maintained at 1.0 A g-1 after 600cycles) and outstanding rate capability (a suitable capacity of 441.7 mAh g-1 was obtained even at 5.0 A g-1). Moreover, the assembled full cell can achieve a capacity of 141.4 mAh g-1 after 65 cycles at 1.0C, exhibiting outstanding cycling stability. This work provides a prospective way for the commercial production of high-performance Si-based anode materials for LIBs.

Thermal Migration Promotes the Formation of Manganese and Nitrogen Doped Polyhedral Surface for Boosted Oxygen Reduction Electrocatalysis.

Increasing the oxygen reduction reaction (ORR) catalytic activity of carbon-based electrocatalysts with robust stability is of great significance for their application. Herein, a feasible thermal migration strategy was proposed to construct manganese- and nitrogen-doped carbonaceous polyhedron frameworks coupled with manganese monoxide microrods (MnO-NC). Mn species were migrated to the surface of polyhedron frameworks, the shape of which was maintained at the high-temperature treatment. The Mn thermal migration not only created highly dispersed Mn-Nx active sites but also promoted graphitization, which benefited ORR electrocatalysis. Moreover, the MnO microrod-supported polyhedron frameworks provide beneficial mass transfer channels for electrocatalysis. Therefore, MnO-NC exhibited impressive ORR catalytic activity and stability in both alkaline and neutral electrolytes compared to commercial Pt/C catalysts. A magnesium-air battery (MAB) driven by MnO-NC delivered a high open circuit voltage and peak power density comparable to that driven by Pt/C. Notably, MnO-NC-driven MAB possessed a longer discharge time than the Pt/C-driven one, indicative of the superior catalytic performance of Mn-NC. This work provides a simple but effective strategy to construct carbonaceous framework electrocatalysts for boosted ORR, promoting the widespread application of metal-air batteries and fuel cells.

Robust Oxygen Reduction Electrocatalysis Enabled by Platinum Rooted on Molybdenum Nitride Microrods.

Robust oxygen reduction electrocatalysis is central to renewable fuel cells and metal-air batteries. Herein, Pt nanoparticles (NPs) rooted on porous molybdenum nitride microrods (Pt/Mo2N MRs) are rationally constructed toward the oxygen reduction reaction (ORR). Owing to the desired composition with strong electronic metal-support interactions (EMSIs) and a porous one-dimensional structure supporting ultrafine NPs, the developed Pt/Mo2N MRs possess much higher ORR mass and specific activities than commercial Pt/C. In situ Raman and density functional theory calculations reveal that the EMSI weakens the adsorption of intermediates over Pt/Mo2N MRs via an associative mechanism. Moreover, the porous Mo2N support stabilizes these high activities. Impressively, a homemade zinc-air battery driven by Pt/Mo2N MRs delivers excellent performance including a peak power density of 167 mW cm-2 and a high rate capability that ranged from 5 to 50 mA cm-2. This work highlights the role of EMSI in promoting robust ORR electrocatalysis, thus providing a promising approach for efficient and robust cathode materials for advanced metal-air batteries.

SnS@C nanoparticles anchored on graphene oxide as high-performance anode materials for lithium-ion batteries.

Tin (II) sulfide (SnS) has been regarded as an attractive anode material for lithium-ion batteries (LIBs) owing to its high theoretical capacity. However, sulfide undergoes significant volume change during lithiation/delithiation, leading to rapid capacity degradation, which severely hinders its further practical application in lithium-ion batteries. Here, we report a simple and effective method for the synthesis of SnS@C/G composites, where SnS@C nanoparticles are strongly coupled onto the graphene oxide nanosheets through dopamine-derived carbon species. In such a designed architecture, the SnS@C/G composites show various advantages including buffering the volume expansion of Sn, suppressing the coarsening of Sn, and dissolving Li2S during the cyclic lithiation/delithiation process by graphene oxide and N-doped carbon. As a result, the SnS@C/G composite exhibits outstanding rate performance as an anode material for lithium-ion batteries with a capacity of up to 434 mAh g-1 at a current density of 5.0 A g-1 and excellent cycle stability with a capacity retention of 839 mAh g-1 at 1.0 A g-1 after 450 cycles.

Diatomite waste derived N-doped porous carbon for applications in the oxygen reduction reaction and supercapacitors.

Biomass waste recycling and utilization is of great significance for improving ecological environments and relieving the current energy crisis. Waste diatomite with an adsorbed mass of yeast protein resulting from beer filtration is feasibly converted into N-doped porous carbon (NPC) via high temperature thermal treatment. The resulting NPC inherits the three-dimensional hierarchical structure of the diatomite, with a unique rich-pore feature composed of micro/meso/macropores, which is beneficial for high exposure of the electrocatalytic sites and ion transfer and diffusion. The NPC compounds with controllable nitrogen doping are used for the oxygen reduction reaction (ORR) and in a supercapacitor. NPC-2 exhibits a half-wave potential of 0.801 V comparable to that (0.812 V) of commercially available Pt/C in alkaline media, along with a good methanol tolerance capacity and long-term stability for the ORR. Furthermore, as an electrode material, a symmetric supercapacitor based on NPC-2 manifests an outstanding specific capacitance of 151.5 F g-1 at a current density of 1 A g-1 and a considerable capacitance retention of 90.5% after a cycling performance test of 10 000 cycles. The NPC-2 based symmetric SC delivered an energy density of 13.47 W h kg-1 at a power density of 400 W kg-1. This work highlights the environmental significance of converting waste diatomite into metal-free ORR catalysts and electrode materials for energy conversion and storage technologies.

A green, efficient, closed-loop direct regeneration technology for reconstructing of the LiNi0.5Co0.2Mn0.3O2 cathode material from spent lithium-ion batteries.

Lithium nickel manganese cobalt oxide in the spent lithium ion batteries (LIBs) contains a lot of lithium, nickel, cobalt and manganese. However, how to effectively recover these valuable metals under the premise of reducing environmental pollution is still a challenge. In this work, a green, efficient, closed-loop direct regeneration technology is proposed to reconstruct LiNi0.5Co0.2Mn0.3O2 (NCM523) cathode materials from spent LIBs. Firstly, the failure mechanism of NCM523 cathode materials in the spent LIBs is analyzed deeply. It is found that the spent NCM523 material has problems such as the dissolution of lithium and transition metals, surface interface failure and structural transformation, resulting in serious deterioration of electrochemical performance. Then NCM523 material was directly regenerated by supplementing metal ions, granulation, ion doping and heat treatment. Meanwhile, PO43- polyanions were doped into the regenerated NCM material in the recovery process, showing excellent electrochemical performance with discharge capacity of 189.8 mAh g-1 at 0.1 C. The recovery process proposed in this study puts forward a new strategy for the recovery various lithium nickel cobalt manganese oxide (e.g., LiNi1/3Co1/3Mn1/3O2, LiNi0.5Co0.2Mn0.3O2, LiNi0.6Co0.2Mn0.2O2 and LiNi0.8Co0.1Mn0.1O2) and accelerates the industrialization of spent lithium ion battery recycling.

FeSe2@C Microrods as a Superior Long-Life and High-Rate Anode for Sodium Ion Batteries.

Transition-metal selenides have emerged as promising anode materials for sodium ion batteries (SIBs). Nevertheless, they suffer from volume expansion, polyselenide dissolution, and sluggish kinetics, which lead to inadequate conversion reaction toward sodium and poor reversibility during the desodiation process. Therefore, the transition-metal selenides are far from long cycling stability, outstanding rate performance, and high initial Coulombic efficiency, which are the major challenges for practical application in SIBs. Here, an efficient anode material including an FeSe2 core and N-doped carbon shell with inner void space as well as high conductivity is developed for outstanding rate performance and long cycle life SIBs. In the ingeniously designed FeSe2@NC microrods, the N-doped carbon shell can facilitate mass transport/electron transfer, protect the FeSe2 core from the electrolyte, and accommodate volume variation of FeSe2 with the help of the inner void of the core. Thus, the FeSe2@NC microrods can maintain strong structural integrity upon long cycling and ensure a good reversible conversion reaction of FeSe2 during the discharge/charge process. As a result, the as-prepared FeSe2@NC microrods exhibit excellent sodium storage performance and ultrahigh stability, achieving an excellent rate capability (411 mAh g-1 at 10.0 A g-1) and a long-term cycle performance (401.3 mAh g-1 after 2000 cycles at 5.0 A g-1).

Airway relaxation mechanisms and structural basis of osthole for improving lung function in asthma.

Overuse of ß2-adrenoceptor agonist bronchodilators evokes receptor desensitization, decreased efficacy, and an increased risk of death in asthma patients. Bronchodilators that do not target ß2-adrenoceptors represent a critical unmet need for asthma management. Here, we characterize the utility of osthole, a coumarin derived from a traditional Chinese medicine, in preclinical models of asthma. In mouse precision-cut lung slices, osthole relaxed preconstricted airways, irrespective of ß2-adrenoceptor desensitization. Osthole administered in murine asthma models attenuated airway hyperresponsiveness, a hallmark of asthma. Osthole inhibited phosphodiesterase 4D (PDE4D) activity to amplify autocrine prostaglandin E2 signaling in airway smooth muscle cells that eventually triggered cAMP/PKA-dependent relaxation of airways. The crystal structure of the PDE4D complexed with osthole revealed that osthole bound to the catalytic site to prevent cAMP binding and hydrolysis. Together, our studies elucidate a specific molecular target and mechanism by which osthole induces airway relaxation. Identification of osthole binding sites on PDE4D will guide further development of bronchodilators that are not subject to tachyphylaxis and would thus avoid ß2-adrenoceptor agonist resistance.

Short-range amorphous carbon nanosheets for oxygen reduction electrocatalysis.

Selectively creating active sites that can work well in different media as much as possible remains an open challenge for the widespread application of sustainable metal air batteries and fuel cells. Herein, short-range amorphous nitrogen-doped carbon nanosheets (NCS) coupled with partially graphitized porous carbon architecture were reported, and were prepared via flexible salt-assisted calcination strategy and followed by a simple cleaning process. The short-range amorphous structure not only significantly promotes the exposure of electrochemically active sites of carbon defects with less protonation in acidic medium, but also maintains the structural stability and electron conduction of the NCS. This unique structure endows the NCS (0.832 V) with efficient ORR electrocatalytic performance with a high half-wave potential (E 1/2) comparable to that of commercial Pt/C (0.837 V) in alkaline electrolyte and an impressive E 1/2 of 0.64 V in harsh acidic medium, making it outstanding among the reported analogous metal-free carbon electrocatalysts. In addition, the NCS manifests robust stability for ORR electrocatalysis with little change in the catalytic activity after accelerated stability tests. This work will provide a feasible inspiration to the construction of carbon nanomaterials with high active site density for efficient energy conversion-related electrochemical reactions.

TiO2 Nanosheet-Redox Graphene Oxide/Sulphur Cathode for High-Performance Lithium-Sulphur Batteries.

Lithium-sulphur batteries are considered as some of the most potent secondary-battery systems. These batteries are expected to have extensive applications in fields requiring high-energy density. However, such applications are hindered by some serious intrinsic obstacles. Herein, TiO2 nanosheets-rGO/sulphur (TiO2 NS-rGO/S) composites were fabricated through a two-process hydrothermal method. TiO2 nanosheets served as active sites for polysulphide absorption, whereas rGO offered space for sulphur improvement and TiO2 NS-rGO/S composites. The TiO2 NS-rGO/S composite exhibited high discharge capacity of 1099 mAh·g-1 at 0.2 C rate and retained a capacity of 690 mAh·g-1 after 100 cycles, with high sulphur loading of 3 mg·cm-2. The high initial specific discharge capacity and improved cyclic stability were attributed to the synergistic effects of TiO2 nanosheets and rGO. These results indicated that the simple, low-cost and scalable method provides a novel perspective on practical utilisation of lithium-sulphur batteries.

Three-dimensional flower-like NiCo2O4/CNT for efficient catalysis of the oxygen evolution reaction.

The oxygen evolution reaction (OER) is an important reaction especially in water splitting and metal-air batteries. Highly efficient non-noble metal based electrocatalysts are urgently required to be developed and to replace the commercial Ru/Ir based oxide. Herein, we report the three-dimensional hierarchical NiCo2O4/CNT-150 composite with high activity for the OER that was synthesized via a hydrothermal reaction and subsequent annealing. Compared with CNTs, commercial RuO2 catalysts, NiCo2O4/CNT, NiCo2O4/CNT-250, and NiCo2O4/CNT-150 exhibit enhanced electrocatalytic performance with a lower onset overpotential of 300 mV and the corresponding Tafel slope of 129 mV per decade. The flower-like NiCo2O4/CNT-150 shows an excellent catalysis performance with higher current density than the commercial RuO2 catalyst. Moreover, the NiCo2O4/CNT-150 demonstrates the excellent long-term durability in 0.1 mol L-1 KOH for the OER. The significant catalytic performances are ascribed to the excellent conductivity of CNTs and the high specific surface area of the three dimensional flower-like NiCo2O4.

A New Strategy to Stabilize Capacity and Insight into the Interface Behavior in Electrochemical Reaction of LiNi0.5Mn1.5O4/Graphite System for High-Voltage Lithium-Ion Batteries.

The performance of CEI and SEI configuration and formation mechanism on the cathode and anode side for LiNi0.5Mn1.5O4/natural graphite (LNMO/NG) batteries is investigated, where series permutations of the NG electrodes modified with TEOS species as the anode for the LNMO full cells. It is believed that the excellent long-term cycling performance of LNMO/NG full cells at the high voltage is a result of alleviating the devastated reaction to form the CEI and SEI on the both electrodes with electrolyte, respectively. At a voltage range from 3.4 to 4.8 V for the LNMO full cells, 95.0% capacity retention after 100 cycles is achieved when cycled with TEOS-modifying NG anode. This mechanism may be explained that eliminating the HF and absorbing water impurities in the electrolyte by introducing the TEOS group, which can transform the SiO2 species that react with the acid of HF at the organic solvent environment instead of destroying/forming the anode SEI and attacking the LNMO spinel structure to form the dense and high resistance CEI, meanwhile the SiO2 species will absorb the water molecule and precipitate into the anode surface further stabilizing the SEI configuration during the cycling.

Three-Dimension Hierarchical Al2O3 Nanosheets Wrapped LiMn2O4 with Enhanced Cycling Stability as Cathode Material for Lithium Ion Batteries.

A three dimensional (3D) Al2O3 coating layer was synthesized by a facile approach including stripping and in situ self-assembly of γ-AlOOH. The uniform flower-like Al2O3 nanosheets with high specific area largely sequesters acidic species produced by side reaction between electrode and electrolyte. The inner coating layer wrapping spinel LiMn2O4 effectively inhibits the dissolution of Mn by suppressing directive contact with electrolyte to enhance cycling stability. The rate performance is improved because of the better electrolyte storage of the assembled hierarchical architecture of the 3D coating layer affording unimpeded Li(+) diffusion from electrode to electrolyte. The electrochemical results reveal the as-prepared coated LiMn2O4 sample with the amount of Al2O3 at 1 wt % exhibits superior cycle stability under room temperature even at elevated temperature. The initial specific discharge capacity is 128.5 mAh g(-1) at 0.1 C and retains 89.8% of the initial capacity after 800 cycles at 1 C rate. When cycling at 55 °C, the composite shows 93.6% capacity retention after 500 cycles. This facile surface modification and effective structure of coating layer can be adopted to enhance the cycling performance and thermal stability of other electrode materials for which Al2O3 plays its role.

Epidermal growth factor-ferritin H-chain protein nanoparticles for tumor active targeting.

Human ferritin H-chain protein (FTH1)-based nanoparticles possess a precisely assembled nanometer-scale structure and high safety. However, their applications for imaging and drug delivery towards cancer cells remain limited due to a lack of target specificity. Epidermal growth factor receptor (EGFR) is overexpressed in many malignant tissues including breast cancer, and has been used as a therapeutic target for cancer treatment. Herein, a genetic method is shown to generate EGF-FTH1 chimeric proteins. EGF-FTH1 nanoparticles with EGF on the surface are then produced. The data demonstrate that EGF-FTH1 nanoparticles, with a small size (11.8 ± 1.8 nm), narrow size distribution, and high biosafety, can specifically bind to and then be taken up by breast cancer MCF-7 cells and MDA-MB-231 cells, but not normal breast epithelial MCF-10A cells. In contrast, binding and absorption of nontargeted ferritin-based nanoparticles to breast cancer cells are negligible. In vivo studies show that EGF-FTH1 nanoparticles are accumulated in breast tumors in a mouse xenograft model. Interestingly, the concentration of EGF-FTH1 nanoparticles in the tumor site is significantly reduced when mice are pretreated with an excess of free EGF. These results imply that EGF-EGFR interaction plays an important role in regulating the tumor retention of EGF-FTH1 nanoparticles.

Characterization of the ATPase activity of a novel chimeric fusion protein consisting of the two nucleotide binding domains of MRP1.

Nucleotide Binding Domains (NBDs) are responsible for the ATPase activity of the multidrug resistance protein 1 (MRP1). A series of NBD1-linker-NBD2 chimeric fusion proteins were constructed, expressed and purified, and their ATPase activities were analyzed. We report here that a GST linked NBD1(642-890)-GST-NBD2(1286-1531) was able to hydrolyze ATP at a rate of about 4.6 nmol/mg/min (K(m)=2.17 mM, V(max)=12.36 nmol/mg/min), which was comparable to the purified and reconstituted MRP1. In contrast, neither a mixture of NBD1 and GST-NBD2 nor the NBD1-GST-NBD1 fusion protein showed detectable ATPase activity. Additionally, the E1455Q mutant was found to be nonfunctional. Measurements by both MIANS labeling and circular dichroism spectroscopy revealed significant conformational differences in the NBD1-GST-NBD2 chimeric fusion protein compared to the mixture of NBD1 and GST-NBD2. The results suggest a direct interaction mediated by GST between the two NBDs of MRP1 leading to conformational changes which would enhance its ATPase activity.

Palmitoylation modification of Galpha(o) depresses its susceptibility to GAP-43 activation.

Interaction between GAP-43 (growth associated protein-43) and Galpha(o) (alpha subunit of Go protein) influences the signal transduction pathways leading to differentiation of neural cells. GAP-43 is known to increase guanine nucleotide exchange by Galpha(o), which is a major component of neuronal growth cone membranes. However, it is not clear whether GAP-43 stimulation is related to the Galpha(o) palmitoylation or the conversion of Galpha(o) from oligmers to monomers, which was shown to be a necessary regulatory factor in GDP/GTP exchange of Galpha(o). Here we expressed and purified GAP-43, GST-GAP-43 and Galpha(o) proteins, detected their stimulatory effect on [(35)S]-GTPgammaS binding of Galpha(o). It was found that the EC(50) of both GAP-43 and GST-GAP-43 activation were tenfold lower in case of depalmitoylated Galpha(o) than palmitoylated Galpha(o). Non-denaturing gel electrophoresis and p-PDM cross-linking analysis revealed that addition of GST-GAP-43 induced disassociation of depalmitoylated Galpha(o) from oligomers to monomers, but did not influence the oligomeric state of palmitoylated Galpha(o), which suggests that palmitoylation is a key regulatory factor in GAP-43 stimulation on Galpha(o). These results indicated the interaction of GAP-43 and Galpha(o) could accelerate conversion of depalmitoylated Galpha(o) but not palmitoylated Galpha(o) from oligomers to monomers, so as to increase the GTPgammaS binding activity of Galpha(o). Results here provide new evidence about how signaling protein palmitoylation is involved in the G-protein-coupled signal transduction cascade, and give a useful clue on the participation of GAP-43 in G-protein cycle by its preferential activation of depalmitoylated Galpha(o).

A role for lipid droplets in inter-membrane lipid traffic.

All cells have the capacity to accumulate neutral lipids and package them into lipid droplets. Recent proteomic analyses indicate that lipid droplets are not simple lipid storage depots, but rather complex organelles that have multiple cellular functions. One of these proposed functions is to distribute neutral lipids as well as phospholipids to various membrane-bound organelles within the cell. Here, we summarize the lipid droplet-associated membrane-trafficking proteins and review the evidence that lipid droplets interact with endoplasmic reticulum, endosomes, peroxisomes, and mitochondria. Based on this evidence, we present a model for how lipid droplets can distribute lipids to specific membrane compartments.