Positive and negative thermophoresis in fluids has found widespread applications from mass transport to molecule manipulation. In solids, although positive thermophoresis has been recently discovered in both theoretical and experimental studies, negative thermophoresis has never been reported. Here we reveal via molecular dynamics simulations that negative thermophoresis does exist in solids. We consider the motion of a single walled carbon nanotube nested inside of two separate outer tubes held at different temperatures. It is found that a sufficiently long inner tube will undergo negative thermophoresis, whereas positive thermophoresis is favorable for a relatively short inner tube. Mechanisms for the observed positive thermophoresis and negative thermophoresis are shown to be totally different. In positive thermophoresis, the driving force comes mainly from the thermally induced edge force and the interlayer attraction force, whereas the driving force for negative thermophoresis is mainly due to the thermal gradient force. These findings have enriched our knowledge of the fundamental driving mechanisms for thermophoresis in solids and may stimulate its further applications in nanotechnology.
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http://dx.doi.org/10.1021/acs.nanolett.6b02815 | DOI Listing |
Front Microbiol
November 2024
Department of Biomedical Sciences, Institute of Biostructures and Bioimaging, National Research Council (CNR), Napoli, Italy.
Introduction: Antimicrobial-resistant pathogens are an ongoing threat to human and animal health. According to the World Health Organization (WHO), colistin is considered the last resort antibiotic against human infections due to multidrug-resistant Gram-negative organisms-including , a priority-1 pathogen. Despite colistin being considered a last resort antibiotic, transferable bacterial resistance to this drug has been reported in humans and animals.
View Article and Find Full Text PDFCurr Microbiol
November 2024
School of Medicine, Nanjing University of Chinese Medicine, 138 Xianlin Rd, Nanjing, 210023, People's Republic of China.
Bacterial antimicrobial resistance (AMR), particularly multidrug resistance (MDR) in gram-negative bacterial strains, has emerged as a formidable challenge of substantial consequence, necessitating an urgent pursuit of a sustainable and efficacious strategic response. Repurposing nonantibiotic drugs as potential antibiotics or antibiotic adjuvants is a valuable approach to targeting MDR bacteria. A total of 1,750 FDA-approved drugs (APExBIO, USA) were screened to test their antimicrobial activities against MDR bacteria using the broth microdilution method according to the standard of the Clinical and Laboratory Standards Institute (CLSI).
View Article and Find Full Text PDFPlants (Basel)
October 2024
Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Pepper ( L.) suffers severe quality and yield loss from oomycete diseases caused by . CaSGT1 was previously determined to positively regulate the immune response of pepper plants against , but by which mechanism remains elusive.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2024
Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400715, China.
Endosymbionts provide essential nutrients for hosts, promoting growth, development, and reproduction. However, the molecular regulation of nutrient transport from endosymbiont to host is not well understood. Here, we used bioinformatic analysis, RNA-Sequencing, luciferase assays, RNA immunoprecipitation, and in situ hybridization to show that a bacteriocyte-distributed gene (multidrug resistance-associated protein 4) is negatively regulated by a host (aphid)-specific microRNA (miR-3024).
View Article and Find Full Text PDFChin Med J (Engl)
October 2024
The First Department of General Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, Gansu 730000, China.
Background: Gastric cancer (GC), a malignant tumor with poor prognosis, is one of the leading causes of cancer-related deaths worldwide; consequently, identifying novel therapeutic targets is crucial for its corresponding treatment. NUF2 , a component of the NDC80 kinetochore complex, promotes cancer progression in multiple malignancies. Therefore, this study aimed to explore the potential of NUF2 as a therapeutic target to inhibit GC progression.
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