Toggle light / dark theme

Some of the more well-known examples include retrievable and reusable rockets, retrieval at sea, mid-air retrieval, single-stage-to-orbit (SSTO) rockets, and kinetic launch systems.

In addition, there are also efforts to develop propulsion systems that do not rely on conventional propellants. This technology offers many advantages, including lower mass and improved energy efficiency, ultimately lowering costs.

On June 10, 2023, an all-electrical propulsion system for satellites (the IVO Quantum Drive) will fly to space for the first time. The system was built by North Dakota-based wireless power company IVO, Ltd. and will serve as a testbed for an alternative theory of inertia that could have applications for propulsion.

Researchers at University of Oxford have recently created a quantum memory within a trapped-ion quantum network node. Their unique memory design, introduced in a paper in Physical Review Letters, has been found to be extremely robust, meaning that it could store information for long periods of time despite ongoing network activity.

“We are building a network of quantum computers, which use trapped ions to store and process quantum information,” Peter Drmota, one of the researchers who carried out the study, told Phys.org. “To connect quantum processing devices, we use emitted from a single atomic ion and utilize between this ion and the photons.”

Trapped ions, charged atomic particles that are confined in space using , are a commonly used platform for realizing quantum computations. Photons (i.e., the particles of light), on the other hand, are generally used to transmit quantum information between distant nodes. Drmota and his colleagues have been exploring the possibility of combining trapped ions with photons, to create more powerful quantum technologies.

Macromolecular machines acting on genes are at the core of life’s fundamental processes, including DNA replication and repair, gene transcription and regulation, chromatin packaging, RNA splicing, and genome editing. Here, we report the increasing role of computational biophysics in characterizing the mechanisms of “machines on genes”, focusing on innovative applications of computational methods and their integration with structural and biophysical experiments. We showcase how state-of-the-art computational methods, including classical and ab initio molecular dynamics to enhanced sampling techniques, and coarse-grained approaches are used for understanding and exploring gene machines for real-world applications.

The story of modern physics has been one of reductionism. We do not need a vast encyclopedia to understand the inner workings of Nature. Rather, we can describe a near-limitless range of natural phenomena, from the interior of a proton to the creation of galaxies, with apparently unreasonable efficiency using the language of mathematics. In the words of theoretical physicist Eugene Wigner, ‘The miracle of the appropriateness of the language of mathematics for the formulation of the laws of physics is a wonderful gift which we neither understand nor deserve. We should be grateful for it.’

The mathematics of the twentieth century described a Universe populated by a limited number of different types of fundamental particles interacting with each other in an arena known as spacetime according to a collection of rules that can be written down on the back of an envelope. If the Universe was designed, it seemed, the designer was a mathematician.

Today, the study of black holes appears to be edging us in a new direction, towards a language more often used by quantum computer scientists. The language of information. Space and time may be emergent entities that do not exist in the deepest description of Nature. Instead, they are synthesized out of entangled quantum bits of information in a way that resembles a cleverly constructed computer code. If the Universe is designed, it seems, the designer is a programmer.

A recently patented genome editing tool called PASTE holds genuine promise for expanding the universe of treatable genetic diseases. The approach combines elements of CRISPR and prime editing with a pair of enzymes designed to enable the integration of large segments of DNA without incurring double-stranded DNA breaks.

U.S. Patent No. 11,572,556, assigned to MIT, covers systems, methods, and compositions for programmable addition via site-specific targeting elements (PASTE). The patent describes site-specific integration of a nucleic acid into a genome, using a CRISPR–Cas9 nickase fused to a reverse transcriptase (RT) and a serine integrase. These enzymes target specific genome sequences known as attachment sites, binding to them before integrating their DNA payload.

PASTE can insert DNA fragments as large as 50,000 base pairs, which puts it on a different plane compared to other genome editing tools such as prime editing.