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Antimicrobial peptides (AMPs) are a crucial component of the natural defense system that the host employs to protect itself against invading pathogens. PMAP-23, a cathelicidin-derived AMP, has potent and broad spectrum antimicrobial activity. Our earlier studies led us to hypothesize that PMAP-23 adopts a dynamic helix-hinge-helix structure, initially attaching to membrane surfaces through the N-helix and subsequently inserting the C-helix into the lipid bilayer. Here, we rationally designed PMAP-NC with increased amphipathicity and hydrophobicity in the N- and C-helix, respectively, based on the hypothesis of the interaction of PMAP-23 with membranes. Compared to the parental PMAP-23, PMAP-NC showed 2–8 fold improved bactericidal activity against both gram-positive and gram-negative strains with fast killing kinetics. Fluorescence studies demonstrated that PMAP-NC largely disrupted membrane integrity, indicating that efficiency and kinetics of bacterial killing are associated with the membrane permeabilization. Interestingly, PMAP-NC exhibited much better anticancer activity against tumor cells than PMAP-23 but displayed low hemolytic activity against human erythrocytes. Collectively, our findings suggest that PMAP-NC, with the structural arrangement of an amphipathic helix–hinge–hydrophobic helix that plays a critical role in rapid and efficient membrane permeabilization, can be an attractive candidate for novel antimicrobial and/or anticancer drugs.

Antimicrobial peptides (AMPs) that selectively permeabilize bacterial membranes are promising alternatives to conventional antibiotics. Dimerization of AMP is considered an attractive strategy to enhance antimicrobial and membrane-lytic activity, but it also increases undesired hemolytic and cytotoxic activity. Here, we prepared Lys-linked homodimers of membrane-permeabilizing magainin II and cell-penetrating buforin II. Dimerization did not significantly alter conformational behavior, but it had a substantial impact on antimicrobial properties. We found that while the magainin II dimer showed increased antimicrobial and cytotoxic effects, the buforin II dimer conferred much greater antibacterial potency without exhibiting cytotoxic activity. Interestingly, the buforin II dimer was highly effective against several antibiotic-resistant bacterial isolates. Membrane permeabilization experiments indicated that the magainin II dimer rapidly disrupted both anionic and zwitterionic membranes, whereas the buforin II dimer selectively disrupted anionic membranes. Like the monomeric form, the buforin II dimer was efficiently translocated across lipid bilayers. Therefore, our results suggest that the dimerization of cell-penetrating buforin II not only disrupts the bacterial membrane, but also translocates it across the membrane to target intracellular components, resulting in effective antimicrobial activity. We propose that dimerization of intracellular targeting AMPs may present a superior strategy for therapeutic control of pathogenic bacteria.

Thermochemical heat storage is a promising energy storage method and has received much attention in recent years. To improve the design and application of such systems, a better understanding of the characteristics of thermochemical heat storage is required. In this study, we analyze the heat release characteristics of thermochemical heat storage considering various operating parameters, such as charging temperature, humidity, and material. Three different thermochemical materials are considered herein, namely, zeolite 13X, zeolite 5A, and silica gel. The temperature profile at the inlet and outlet of the storage chamber, and that inside the chamber packed with thermochemical material, were measured. The pressure drop across the chamber was measured as well. The results indicate that the heat release characteristics change with position and time. Furthermore, the temporal curves of released heat are significantly affected by charging temperature and humidity. Zeolite 13X rapidly released a large amount of heat within a short period of time, whereas silica gel gradually released a small amount of heat, over a longer duration of time. The pressure drop across the chamber was found to vary with the bead size of the thermochemical material. Thus, the operating parameters including charging temperature, humidity, and material, have a significant effect on the characteristics of heat release. The data obtained herein can serve as a reference for the design of thermochemical storage systems.

Tokenization is a significant primary step for the training of the Pre-trained Language Model (PLM), which alleviates the challenging Out-of-Vocabulary problem in the area of Natural Language Processing. As tokenization strategies can change linguistic understanding, it is essential to consider the composition of input features based on the characteristics of the language for model performance. This study answers the question of “Which tokenization strategy enhances the characteristics of the Korean language for the Named Entity Recognition (NER) task based on a language model?” focusing on tokenization, which significantly affects the quality of input features. We present two significant challenges for the NER task with the agglutinative characteristics in the Korean language. Next, we quantitatively and qualitatively analyze the coping process of each tokenization strategy for these challenges. By adopting various linguistic segmentation such as morpheme, syllable and subcharacter, we demonstrate the effectiveness and prove the performance between PLMs based on each tokenization strategy. We validate that the most consistent strategy for the challenges of the Korean language is a syllable based on Sentencepiece.

With the regular increase in global solid waste, landfilling is intensively used for waste disposal. However, landfill gas (LFG) produced as a byproduct during waste decomposition in the landfills is a serious problem since it leads to damage to the eco-systems. Accordingly, it has been highlighted to convert LFG into other value-added chemicals. In this study, LFG utilization was studied in terms of conversion into methanol (MeOH) by considering different scenarios of LFG utilization. Techno-economic analysis and environmental assessment were performed to identify the economic feasibility and environmental impact of each case. From the economic analysis, bio-MeOH production costs of 879.16, 724.52, and 1,130.74 $ ton

Cross-linking technology has been considered as one of the effective strategies for improving the physicochemical stability of proton-exchange membranes (PEMs) for fuel cell applications. However, ...

An optimized acid hydrolysis method was developed to yield carboxylic acid-functionalized PIM-1 (PIM-COOH) with >89% conversion in 48 h using a postpolymerization reaction of PIM-1. Physical charac...

Nanotube membranes could show significantly enhanced permeance and selectivity for gas separations. Up until now, studies have primarily focused on applying carbon nanotubes to membranes to achieve...

Antimicrobial peptides (AMPs), essential elements in host innate immune defenses against numerous pathogens, have received considerable attention as potential alternatives to conventional antibiotics. Most AMPs exert broad-spectrum antimicrobial activity through depolarization and permeabilization of the bacterial cytoplasmic membrane. Here, we introduce a new approach for enhancing the antibiotic activity of AMPs by conjugation of a cationic cell-penetrating peptide (CPP). Interestingly, CPP-conjugated AMPs elicited only a 2- to 4-fold increase in antimicrobial activity against Gram-positive bacteria, but showed a 4- to 16-fold increase in antimicrobial activity against Gram-negative bacteria. Although CPP–AMP conjugates did not significantly increase membrane permeability, they efficiently translocated across a lipid bilayer. Indeed, confocal microscopy showed that, while AMPs were localized mainly in the membrane of Escherichia coli, the conjugates readily penetrated bacterial cells. In addition, the conjugates exhibited a higher affinity for DNA than unconjugated AMPs. Collectively, we demonstrate that CPP–AMP conjugates possess multiple functional properties, including membrane permeabilization, membrane translocation, and DNA binding, which are involved in their enhanced antibacterial activity against Gram-negative bacteria. We propose that conjugation of CPPs to AMPs may present an effective approach for the development of novel antimicrobials against Gram-negative bacteria.

The effect of repair patches with different geometric shapes on bonding strength was investigated. Four shapes of patches were considered: rectangular patch (RP), triangular patch (TP), inv...

End-group cross-linked sulfonated poly(arylene ether sulfone) (SPAES) membranes were prepared using thiol capped SPAES (SH-SPAES) with different amounts of vinyl polysulfone (VPSf) as a polymeric cross-linker. The cross-linked membranes showed remarkably improved physicochemical stabilities compared to the corresponding linear SPAES membrane. Although the proton conductivity of the SPAES membrane composed of SPAES with the degree of sulfonation (DS) as 70 mol% could not be measured due to its low physical stability under the measurement condition, those of the cross-linked membranes were repeatedly evaluated due to the enhanced stability through the formation of cross-linked structures. The obtained proton conductivity values from cross-linked membranes are larger than those of the linear SPAES membrane which composed of SPAES with DS of 50 mol% having the ion exchange capacity (IEC) similar to that of the cross-linked membranes, especially at relative low humidity conditions. Furthermore, the fuel cell performance of the membrane electrode assembly (MEA) prepared with the cross-linked membrane, showing the optimized physicochemical stabilities and proton conductivity exhibited a maximum power density of 692 mW cm−2, which was larger than that with Nafion 212 (603 mW cm−2) at 80 °C under fully humidified H2/Air condition.

Sulfonated poly(arylene ether sulfone) (SPAES) composite membranes were prepared using graphene oxide (GO) and sulfonated poly(arylene thioether sulfone)-grafted graphene oxide (SATS-GO) as fillers for proton exchange membrane fuel cell (PEMFC) applications. When GO and SATS-GO were mixed with SPAES to form the composite membranes, dimensional stability, chemical stability, and mechanical strength were improved. The composite membranes containing SATS-GO especially showed higher proton conductivity than the pristine SPAES and the composite membrane containing GO because of highly sulfonated polymer (SATS) introduced on GO surface. Furthermore, the sulfonic acid groups in SATS-GO can increase the compatibility between the filler and matrix polymer.

To reduce CO2 emissions and address climate change concerns, most futuristic studies investigating 100% renewable energy sources and subsequent power-to-gas/fuel/liquid/X technological developments have been based on hydrogen (H2). The long-term storage and transportation of H2 over long distances restrict its feasibility as an energy vector, mainly due to its low energy density. Liquefaction is a promising approach for overcoming these issues. However, it requires a large amount of energy, and if H2 itself is used to provide this energy, then 25% to 35% of the initial quantity of H2 is consumed. The existing H2 liquefaction plants have specific energy consumption values in the range of 10–12 kWh / kg LH 2 and exergy efficiencies in the range of 20%–30% with complicated configurations. Therefore, a thermodynamically efficient and compact design is required to facilitate a roadmap to H2 economy. This paper proposes a simple, energy-efficient, and cost-effective process for H2 liquefaction. Three refrigeration cycles with optimal mixed-refrigerant compositions are used, which makes the proposed process energy-efficient. Additionally, two-stage ortho-to-para conversion makes the process compact. The proposed process is unique in terms of its configuration and mixed-refrigerant combination. The modified coordinate descent approach was adopted to identify the optimal design variables for the proposed H2 liquefaction process. The proposed process consumes an energy of 6.45 kWh / kg LH 2 , which is 36.5% and 16.1% lower than that consumed by the base design of the proposed process and a published base case, respectively. Additionally, the exergy efficiency of the proposed process is 47.2%. This study will help process engineers achieve a sustainable green economy by improving the competitiveness of H2 storage and transportation over long distances.

Porous nanosheets made of effectively aligned zeolitic imidazolate framework-8 (ZIF-8), dubbed ZPGO, with an exceptionally high surface area (2170 m2 g−1) were demonstrated. This composite was prepared by growing ZIF-8s on highly porous graphene oxide (PGO) and the mixed matrix membrane with such a nanofiller showed drastically improved size-selective CO2 transport even at very low filler concentration (0.02 wt%) especially under mixed gas conditions where both selectivity (CO2/N2 ∼57) and CO2 permeability (∼163 barrer) were significantly enhanced. In addition to this, ZPGO effectively suppressed CO2-plasticization, which indicates great potential in real operations. This new concept of nanofillers is expected to maximize the filler effect in other fields benefitting from a high surface area as well.

We investigated the effect of graphene oxide (GO) and sulfonated polytriazole grafted graphene oxide (SPTA-GO) on sulfonated poly(arylene ether sulfone) (SPAES) based polymer electrolytes for application in proton exchange membrane fuel cells. GO was fabricated by the chemical oxidation of graphite and SPTA-GO was prepared via the click reaction using copper (Ⅰ) catalyzed azide-alkyne 1,3-dipolar cycloaddition between ethynyl-terminated sulfonated polytriazole (E-SPTA) and azide functionalized GO (N3-GO). All the SPAES based composite membranes with GO and SPTA-GO revealed better physical/chemical stabilities and mechanical strength than the pristine SPAES membrane, while noticeable improvement of proton conductivity was only observed in the SPAES composite membrane with SPTA-GO since the SPTA moiety attached on GO has both sulfonic acid and triazole groups that can introduce the additional proton conducting channels into the SPAES matrix. The maximum power density of the membrane electrode assembly employing the SPAES composite membrane with SPTA-GO reached up to 1.58 W cm−2 at 80 °C and 100% RH condition, which is larger than that employing commercial Nafion 212 (1.33 W cm−2).

Soft and still responsive Transparent touch screens, from large-panel interactive information maps to advanced cell phones, have become a part of daily life. However, such devices all use hard materials. Kim et al. have developed a soft touch panel based on polyacrylamide hydrogels (cross-linked polymers swollen with water) that are highly transparent and contain trapped LiCl to enhance conductivity. The hydrogels are soft and can be stretched extensively while still maintaining touch sensitivity. Science , this issue p. 682