New theory suggests black holes may have “hair” to solve the information paradox.
Scientists at Penn Engineering have developed a quantum sensing method that detects signals from individual atoms.
A surprising class of blood cell not typically associated with immunity plays a role in shaping the durability of immunity to vaccination, new research suggests.
🧬 🧑🏻🔬 By Prof. Itzhak Fishov, et al.
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Phenotypic variability in isogenic bacterial populations is a remarkable feature that helps them cope with external stresses, yet it is incompletely understood. This variability can stem from gene expression noise and/or the unequal partitioning of low-copy-number freely diffusing proteins during cell division. Some high-copy-number components are transiently associated with almost immobile large assemblies (hyperstructures) and may be unequally distributed, contributing to bacterial phenotypic variability. We focus on the nucleoid hyperstructure containing numerous DNA-associated proteins, including the replication initiator DnaA. Previously, we found an increasing asynchrony in the nucleoid segregation dynamics in growing E. coli cell lineages and suggested that variable replication initiation timing may be the main cause of this phenomenon.
From the early days of quantum mechanics, scientists have thought that all particles can be categorized into one of two groups—bosons or fermions—based on their behavior.
However, new research by Rice University physicist Kaden Hazzard and former Rice graduate student Zhiyuan Wang shows the possibility of particles that are neither bosons nor fermions. Their study, published in Nature, mathematically demonstrates the potential existence of paraparticles that have long been thought impossible.
“We determined that new types of particles we never knew of before are possible,” said Hazzard, associate professor of physics and astronomy.
Decoding 2D material growth: White graphene insights open doors to cleaner energy and more efficient electronics
Posted in chemistry, computing, nanotechnology, particle physics | Leave a Comment on Decoding 2D material growth: White graphene insights open doors to cleaner energy and more efficient electronics
A breakthrough in decoding the growth process of hexagonal boron nitride (hBN), a 2D material, and its nanostructures on metal substrates could pave the way for more efficient electronics, cleaner energy solutions and greener chemical manufacturing, according to new research from the University of Surrey published in the journal Small.
Only one atom thick, hBN—often nicknamed “white graphene”—is an ultra-thin, super-resilient material that blocks electrical currents, withstands extreme temperatures and resists chemical damage. Its unique versatility makes it an invaluable component in advanced electronics, where it can protect delicate microchips and enable the development of faster, more efficient transistors.
Going a step further, researchers have also demonstrated the formation of nanoporous hBN, a novel material with structured voids that allows for selective absorption, advanced catalysis and enhanced functionality, vastly expanding its potential environmental applications. This includes sensing and filtering pollutants—as well as enhancing advanced energy systems, including hydrogen storage and electrochemical catalysts for fuel cells.
Autophagy, the cell’s essential housekeeping process, involves degrading and recycling damaged organelles, proteins, and other components to prevent clutter. This vital mechanism, found in all life forms from single-celled organisms to plants and animals, is key to maintaining cellular homeostasis. Its disruption is linked to many known diseases in humans, such as Alzheimer’s, Parkinson’s, and cancer.
Though understanding autophagy in detail is important from medical and biological perspectives, it is not a one-size-fits-all process. There are several forms of autophagy that differ in how the components to be degraded are transported to the lysosomes or vacuoles—the organelles that serve as the cell’s waste disposal and recycling centers.
Autophagy targets a range of intracellular components, including a part of the nucleus that stores important chromosomes. However, the physiological significance of autophagic degradation of the nucleus remains unknown.