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The authors employ computational protein design to identify a mini-protein with the potential to enhance binding of the tight junction protein, claudin-5, at the blood-blood barrier with therapeutic potential for neurodegenerative diseases.

The authors looked how different working conditions impacted the microbiome of the human skin.

In this study, the authors test new antimicrobials by measuring the ability of extracts from Australian-native Myrtaceae species to induce death of two bacteria S. aureus and P. aeruginosa.

This study investigated how 18 commonly used cosmetic products affect the growth of two skin-resident bacteria, Staphylococcus epidermidis and Micrococcus luteus. At higher concentrations, half of the tested products inhibited at least one bacterial species, suggesting that some cosmetics may disrupt the skin microbiome and its natural balance.

The authors compare air quality in the presence and absence of a living wall in a high school hallway in Brooklyn, NY.

The authors identify disinfectant-resistant bacterial strains of infection-causing bacteria from samples collected at a hospital setting.

In this article the authors look at the lung microbiome in patients with cystic fibrosis to determine what the major bacterial species present are.

In this study, the authors investigate the disinfectant potential of many household spices and minerals. More specifically, they test whether these compounds can be used to disinfect mobile phones after daily use with the hope of identifying environmentally-friendly cleaning options.

Here, recognizing the important role of bacterial biofilms in many life-threatening chronic infections, the authors investigated the effectiveness of a combination treatment on biofilms composed of up to three different common species within the lungs of cystic fibrosis patients with computational analysis. They found that a triple cocktail therapy targeting three different signaling pathways has significant potential as both a treatment and prophylaxis.

In this study, the authors design a series of new biaryl small molecules to target and block the binding pocket of the enzyme dihydropteroate synthase, which is important for prokaryotic biosynthesis of folic acid and could serve as better antimicrobial compounds.