Lifeboat Foundation

For decades, researchers have sought ways to precisely manipulate and identify individual molecules like DNA in liquid environments. Such capabilities could revolutionize areas ranging from disease diagnosis to drug development. However, the randomness of molecular movements in fluids has hindered progress.

Now, scientists from Shenzhen University and the Chinese University of Hong Kong report promising advances in optical tweezing techniques that allow exquisite control over nanoscale biological particles (Light: Science & Applications, “CRISPR-powered optothermal nanotweezers: Diverse bio-nanoparticle manipulation and single nucleotide identification”).

A The diagrammatic sketch of the three components in the solution: DNA@AuNS conjugate, CRISPR/Cas12a complex, and target ssDNA. b Optical setup, the BS, SPF, and TL are beam splitter, short pass filter, and tube lens (f = 200 mm), respectively. Additional details of the setup are provided in the Materials and Methods section. c Dispersion of the three components in the solution without optical heating. d Optothermal net force induced migration and DNA@AuNS conjugate cleavage upon optical heating, the heating laser power is 0.5 mW. e Observation of the cleavage after the optical heating is switched off. (© Light: Science & Applications) (click on image to enlarge)

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MIT researchers and colleagues have demonstrated a way to precisely control the size, composition, and other properties of nanoparticles key to the reactions involved in a variety of clean energy and environmental technologies. They did so by leveraging ion irradiation, a technique in which beams of charged particles bombard a material.

They went on to show that nanoparticles created this way have superior performance over their conventionally made counterparts.

“The materials we have worked on could advance several technologies, from fuel cells to generate CO₂-free electricity to the production of clean hydrogen feedstocks for the chemical industry [through electrolysis cells],” says Bilge Yildiz, leader of the work and a professor in MIT’s Department of Nuclear Science and Engineering and Department of Materials Science and Engineering.

Autoimmune disorders are among the most prevalent chronic diseases across the globe. Emerging treatments for autoimmune disorders focus on “adoptive cell therapies,” or those using cells from a patient’s own body to achieve immunosuppression. These therapeutic cells are recognized by the patient’s body as “self,” therefore limiting side effects, and are specifically engineered to localize the intended therapeutic effect.

In treating autoimmune diseases, current adoptive cell therapies have largely centered around the regulatory T cell (T_reg), which is defined by the expression of the Forkhead box protein 3, orFoxp3. Although T_regs offer great potential, using them for therapeutic purposes remains a major challenge. In particular, current delivery methods result in inefficient engineering of T cells.

T_regs only compose approximately 5%–10% of circulating peripheral blood mononuclear cells. Furthermore, T_regs lack more specific surface markers that differentiate them from other T cell populations. These hurdles make it difficult to harvest, purify and grow T_regs to therapeutically relevant numbers. Although there are additional tissue-resident T_regs in non-lymphoid organs such as in skeletal muscle and visceral adipose tissue, these T_regs are severely inaccessible and low in number.

The human mind is by far one of the most amazing natural phenomena known to man. It embodies our perception of reality, and is in that respect the ultimate observer. The past century produced monumental discoveries regarding the nature of nerve cells, the anatomical connections between nerve cells, the electrophysiological properties of nerve cells, and the molecular biology of nervous tissue. What remains to be uncovered is that essential something – the fundamental dynamic mechanism by which all these well understood biophysical elements combine to form a mental state. In this chapter, we further develop the concept of an intraneuronal matrix as the basis for autonomous, self–organized neural computing, bearing in mind that at this stage such models are speculative. The intraneuronal matrix – composed of microtubules, actin filaments, and cross–linking, adaptor, and scaffolding proteins – is envisioned to be an intraneuronal computational network, which operates in conjunction with traditional neural membrane computational mechanisms to provide vastly enhanced computational power to individual neurons as well as to larger neural networks. Both classical and quantum mechanical physical principles may contribute to the ability of these matrices of cytoskeletal proteins to perform computations that regulate synaptic efficacy and neural response. A scientifically plausible route for controlling synaptic efficacy is through the regulation of neural transport of synaptic proteins and of mRNA. Operations within the matrix of cytoskeletal proteins that have applications to learning, memory, perception, and consciousness, and conceptual models implementing classical and quantum mechanical physics are discussed. Nanoneuroscience methods are emerging that are capable of testing aspects of these conceptual models, both theoretically and experimentally. Incorporating intra–neuronal biophysical operations into existing theoretical frameworks of single neuron and neural network function stands to enhance existing models of neurocognition.

Pancreatic cancer is one of the deadliest types of cancers in humans. It is the fourth leading cause of cancer-related deaths in the western world. The early stages of the disease often progress without symptoms, so diagnosis is usually very late.

Another problem: Advanced tumors – and their metastases – can no longer be completely removed. Chemotherapies, in turn, attack not only the tumor cells but also healthy cells throughout the body. Innovative nanoparticles could be a new approach to treat cancer more precisely.

The approach was developed by a research team from the Max Planck Institute (MPI) for Multidisciplinary Sciences, the University Medical Center Göttingen (UMG), and the Karlsruhe Institute of Technology (KIT). The therapy is now to be optimized for clinical application as quickly as possible.

A color wheel (CW) is one of the most essential devices for contemporary projection displays because it provides the color initialization definition and determines the color performance of the whole system. However, conventional color wheels remain limited in terms of color performance and efficiency because of the light-absorbing material and time sequential color generation. Quantum dots, found in 1981 and known as a kind of quasi-zero-dimensional nanomaterial, exhibit excellent features for displays due to their quantum confinement effect, which won the 2023 Nobel Prize in Chemistry. Inspired by this, the paper systematically demonstrates a quantum-dot color wheel (QD-CW) device through theoretical derivation, simulation analysis, and experimental verification. The theoretical model to define the duty circle ratio is presented for the QD-CW and verified by Monte Carlo ray-tracing simulation. In terms of experimental verification, the QD-CW device is realized by multiple rounds of a photolithography process, and then assembled into a blue laser pumped projection prototype for full-color display. The chromaticity coordinates of white-balanced output are finally located at (0.317,0.338), which matches well with a standard D65 source. The color gamut area of the QD-CW device reaches 116.6% NTSC, and the average light conversion efficiency (LCE) of the prepared QD-CW is 57.0%. The proposed QD-CW device has ∼40% higher color gamut area and 1.2× higher LCE than a conventional CW device. These exciting findings show a groundbreaking approach to color generation in projection displays, which are expected to shed light on other high-quality display applications.

Scientists have found that light-activated oxidizing nanoparticles can whiten teeth without causing damage.

Summary: Researchers developed an experimental computing system, resembling a biological brain, that successfully identified handwritten numbers with a 93.4% accuracy rate.

This breakthrough was achieved using a novel training algorithm providing continuous real-time feedback, outperforming traditional batch data processing methods which yielded 91.4% accuracy.

The system’s design features a self-organizing network of nanowires on electrodes, with memory and processing capabilities interwoven, unlike conventional computers with separate modules.