Investigation on cost-effective composites for CO adsorption from post-gasification residue and metal organic framework.

Cost-effective CO adsorbents are gaining increasing attention as viable solutions for mitigating climate change. In this study, composites were synthesized by electrochemically combining the post-gasification residue of Macadamia nut shell with copper benzene-1,3,5-tricarboxylate (CuBTC). Among the different composites synthesized, the ratio of 1:1 between biochar and CuBTC (B 1:1) demonstrated the highest CO adsorption capacity.

CO activation of bamboo residue after hydrothermal treatment and performance as an EDLC electrode.

CO activation of the solid residue of bamboo after hydrothermal treatment, which is used for the production of xylo-oligosaccharide, was investigated in detail. The reference temperature for carbonization and CO activation was 800 °C. The activated carbon from a solid residue was demonstrated to have a higher potential for making EDLC electrodes than bamboo activated carbon thanks to its very low ash content (almost 0) and high porosity structure with a BET surface area up to 2150 m g.

The investigation of activated carbon by KCO activation: Micropores- and macropores-dominated structure.

In this study, the KCO activation of bamboo was investigated in detail, and the structure and properties of the prepared activated carbons were tested for the feasibility of CO capture application and the potential for both ion and bacteria adsorption for use in the field of hazardous wastewater treatment. Activated carbons were produced with different activator ratios, from 0.5 to 6 according to the sample mass ratio.

Conformational instability governed by disulfide bonds partitions the dominant from subdominant helper T-cell responses specific for HIV-1 envelope glycoprotein gp120.

Most individuals infected with human immunodeficiency virus type 1 (HIV-1) generate a CD4(+) T-cell response that is dominated by a few epitopes. Immunodominance may be counterproductive because a broad CD4(+) T-cell response is associated with reduced viral load. Previous studies indicated that antigen three-dimensional structure controls antigen processing and presentation and therefore CD4(+) T-cell epitope dominance.

Comprehensive analysis of contributions from protein conformational stability and major histocompatibility complex class II-peptide binding affinity to CD4+ epitope immunogenicity in HIV-1 envelope glycoprotein.

Unlabelled: Helper T-cell epitope dominance in human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein gp120 is not adequately explained by peptide binding to major histocompatibility complex (MHC) proteins. Antigen processing potentially influences epitope dominance, but few, if any, studies have attempted to reconcile the influences of antigen processing and MHC protein binding for all helper T-cell epitopes of an antigen. Epitopes of gp120 identified in both humans and mice occur on the C-terminal flanks of flexible segments that are likely to be proteolytic cleavage sites.

Tyrosine kinase pathways modulate tumor susceptibility to natural killer cells.

Natural killer (NK) cells are primary effectors of innate immunity directed against transformed tumor cells. In response, tumor cells have developed mechanisms to evade NK cell-mediated lysis through molecular mechanisms that are not well understood. In the present study, we used a lentiviral shRNA library targeting more than 1,000 human genes to identify 83 genes that promote target cell resistance to human NK cell-mediated killing.