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Category: chemistry

Computational framework sheds light on how the brain’s decision-making is impacted in psychiatric disorders

Scientists from the Icahn School of Medicine at Mount Sinai, working in collaboration with a team from the University of Texas at El Paso, have developed a novel computational framework for understanding how a region of the brain known as the striatum is involved in the everyday decisions we make and, importantly, how it might factor into impaired decision-making by individuals with psychiatric disorders like post-traumatic stress disorder and substance use disorder.

In a study published in Nature Communications, the team reported that modulating activity within the striosomal compartment—a neurochemically discrete area of the striatum—might be an important therapeutic strategy for promoting healthier in people with psychiatric disorders.

“Though it has been established that the striatum is clearly important for cost-benefit decision-making, the precise role of the striosomal compartment has remained elusive,” says Ki Goosens, Ph.D., Associate Professor of Pharmacological Sciences and Psychiatry, at the Icahn School of Medicine at Mount Sinai and co-lead author of the study.

AI breakthrough designs peptide drugs to target previously untreatable proteins

A study published in Nature Biotechnology reveals a powerful new use for artificial intelligence: designing small, drug-like molecules that can stick to and break down harmful proteins in the body — even when scientists don’t know what those proteins look like. The breakthrough could lead to new treatments for diseases that have long resisted traditional drug development, including certain cancers, brain disorders, and viral infections.

The study was published on August 13, 2025 by a multi-institutional team of researchers from McMaster University, Duke University, and Cornell University. The AI tool, called PepMLM, is based on an algorithm originally built to understand human language and used in chatbots, but was trained to understand the “language” of proteins.

In 2024, the Nobel Prize in Chemistry was awarded to researchers at Google DeepMind for developing AlphaFold, an AI system that predicts the 3D structure of proteins – a major advance in drug discovery. But many disease-related proteins, including those involved in cancer and neurodegeneration, don’t have stable structures. That’s where PepMLM takes a different approach – instead of relying on structure, the tool uses only the protein’s sequence to design peptide drugs. This makes it possible to target a much broader range of disease proteins, including those that were previously considered “undruggable.”

Cubosome-based method for loading mRNA into exosomes

Exosomes, naturally derived vesicles responsible for intercellular communication, are emerging as next-generation drug delivery systems capable of transporting therapeutics to specific cells. However, their tightly packed, cholesterol-rich membranes make it extremely difficult to encapsulate large molecules such as mRNA or proteins.

Conventional approaches have relied on techniques like electroporation or chemical treatment, which often damage both the drugs and exosomes, reduce delivery efficiency, and require complex purification steps—all of which pose significant barriers to commercialization.

The team utilized a lipid-based nanoparticle known as a “cubosome,” which mimics the fusion structure of cell membranes and naturally fuses with exosomes. By mixing cubosomes carrying mRNA with exosomes at room temperature for just 10 minutes, the researchers achieved efficient fusion and confirmed that the mRNA was successfully loaded into the exosomes. Analysis showed that over 98% of the mRNA was encapsulated, while the structural integrity and biological function of the exosomes were preserved.

Furthermore, the engineered exosomes demonstrated the ability to cross the blood-brain barrier, one of the most difficult hurdles in drug delivery. Notably, the team observed a “homing” effect, where exosomes return to the type of cell they originated from, enabling targeted drug delivery to diseased tissues.

Bioelectrosynthesis platform enables switch-like, precision control of cell signaling

Cells use various signaling molecules to regulate the nervous, immune, and vascular systems. Among these, nitric oxide (NO) and ammonia (NH₃) play important roles, but their chemical instability and gaseous nature make them difficult to generate or control externally.

A KAIST research team has developed a platform that generates specific signaling molecules in situ from a single precursor under an applied electrical signal, enabling switch-like, precise spatiotemporal control of cellular responses. This approach could provide a foundation for future medical technologies such as electroceuticals, electrogenetics, and personalized cell therapies.

The research team led by Professor Jimin Park from the Department of Chemical and Biomolecular Engineering, in collaboration with Professor Jihan Kim’s group, has developed a bioelectrosynthesis platform capable of producing either or on demand using only an electrical signal. The platform allows control over the timing, spatial range, and duration of cell responses.

Molecular hybridization achieved through quantum vacuum manipulation

Interactions between atoms and molecules are facilitated by electromagnetic fields. The bigger the distance between the partners involved, the weaker these mutual interactions are. In order for the particles to be able to form natural chemical bonds, the distance between them must usually be approximately equal to their diameter.

Using an which strongly alters the , scientists at the Max Planck Institute for the Science of Light (MPL) have succeeded for the first time in optically “bonding” several molecules at greater distances. The physicists are thus experimentally creating synthetic states of coupled molecules, thereby establishing the foundation for the development of new hybrid light-matter states. The study is published in the journal Proceedings of the National Academy of Sciences.

Atoms and molecules have clearly defined, discrete energy levels. When they are combined to form a , the energy states change. This process is referred to as molecular hybridization and is characterized by the overlap of electron orbitals, i.e., the areas where electrons typically reside. However, at a scale of a few nanometers, the interaction becomes so weak that molecules are no longer able to communicate with each other.

Tiny robots use sound to self-organize into intelligent groups

Animals like bats, whales and insects have long used acoustic signals for communication and navigation. Now, an international team of scientists has taken a page from nature’s playbook to model micro-sized robots that use sound waves to coordinate into large swarms that exhibit intelligent-like behavior.

The robot groups could one day carry out complex tasks like exploring disaster zones, cleaning up pollution, or performing from inside the body, according to team lead Igor Aronson, Huck Chair Professor of Biomedical Engineering, Chemistry, and Mathematics at Penn State.

“Picture swarms of bees or midges,” Aronson said. “They move, that creates sound, and the sound keeps them cohesive, many individuals acting as one.”

Scientists May Have Finally Found the Strange, Frozen Hideout of Missing Sulfur

Scientists may have found the hiding place of missing cosmic sulfur—in icy space dust, bound in crown-shaped and chain-like molecules that escape detection. For years, scientists studying the chemistry of the cosmos have searched for sulfur in space, only to discover that it appears to be far les

Molecular mechanisms show how the blood-brain barrier gets leakier with age

A new study from researchers at the University of Illinois Chicago reveals how the blood-brain barrier gets leakier with age, contributing to memory deficits. The study, published in Cell Reports, uncovered the molecular mechanisms behind this process and could provide new therapeutic targets to address cognitive decline earlier in the aging process.

The is a layer of cells lining the brain’s blood vessels that keep viruses, bacteria and toxins out while allowing helpful nutrients and chemicals in. A key structure of the blood-brain barrier are tight junctions that act as bridges between cells, restricting entry of molecules. A protein called occludin helps fulfill this essential role.

“It’s a highly regulatable process that allows some molecules to go through and others to remain in circulation,” said Yulia Komarova, UIC associate professor in the department of pharmacology and at the College of Medicine and senior author of the study. “Basically, it’s a mechanism that separates the central nervous system from everything else.”

Unexpected Resonances Could Boost NMR’s Potency

A radio-frequency field can be resonant with nuclear spins in a sample even if its frequency does not match a spectroscopic transition—a result that could enable new forms of NMR spectroscopy.

Physical systems often have characteristic frequencies. When excited at such a frequency, they start to resonate. The Broughton Suspension Bridge incident on April 12, 1831, showed how this can go wrong. A detachment of 74 riflemen marched in step over the bridge, accidentally matching its resonance frequency. Before they had crossed, the bridge collapsed. At the much-smaller scale of nuclear magnetic resonance (NMR) spectroscopy, resonant excitation is less dramatic yet very useful. Typically, NMR relies on secular resonance, which occurs when the energy of the radio-frequency photons used in a measurement matches the energy required for flipping the magnetic moment of a nucleus in a static magnetic field. This secular resonance occurs at the so-called Larmor frequency. Structure determination of chemical compounds, experimental observation of protein dynamics, and magnetic resonance imaging rely on this matching.

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