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Dr. Fan Liu: “Thanks to this very high precision analysis, we can see chemical differences between the twins. This provides very strong evidence that one of the stars has swallowed planets or planetary material and changed its composition.”


Can stars eat planets? This is what a recent study published in Nature hopes to address as a team of international researchers led by ASTRO 3D researchers investigated how some pairs of twin stars possess different compositions, which contradicts longstanding theories that they should possess similar compositions, hence the same twin stars. However, astronomers now hypothesize the compositional differences could be due to one of the twin stars devouring planets that orbit them. This study holds the potential to help astronomers better understand the formation and evolution of planetary systems and the mechanisms behind them, as well.

For the study, the team used a combination of the 6.5-meter Magellan Telescope, the European Southern Observatory’s Very Large Telescope, and the 10-meter Keck Telescope to collect data on 91 twin stars to ascertain their chemical compositions, and specifically the similarity of their compositions. In the end, the team discovered that approximately eight percent (7−8 twin stars) exhibited differences in their compositions, with the team hypothesizing that this was due to one of the stars ingesting one of their orbiting planets. Additionally, they found that the differing pairs were all main sequence stars, meaning they’re average-aged and conducting their fusion at their full potential. For context, our Sun is a main sequence star.

Researchers report the birth of a ~2-billion-year-old orphan gene following #planetary #oxygenation, and how this humble beginning shaped the global planetary #ecosystem.

From so simple, a beginning: https://oup.silverchair-cdn.com/UI/app/svg/i.svg?versionId=192134


Abstract. Molecular innovations within key metabolisms can have profound impacts on element cycling and ecological distribution. Yet, much of the molecular foundations of early evolved enzymes and metabolisms are unknown. Here, we bring one such mystery to relief by probing the birth and evolution of the G-subunit protein, an integral component of certain members of the nitrogenase family, the only enzymes capable of biological nitrogen fixation. The G-subunit is a Paleoproterozoic-age orphan protein that appears more than 1 billion years after the origin of nitrogenases. We show that the G-subunit arose with novel nitrogenase metal dependence and the ecological expansion of nitrogen-fixing microbes following the transition in enviromental metal availabilities and atmospheric oxygenation that began ∼2.5 billion years ago. We identify molecular features that suggest early G-subunit proteins mediated cofactor or protein interactions required for novel metal dependency, priming ancient nitrogenases and their hosts to exploit these newly diversified geochemical environments. We further examined the degree of functional specialization in G-subunit evolution with extant and ancestral homologs using laboratory reconstruction experiments. Our results indicate that permanent recruitment of the orphan protein depended on the prior establishment of conserved molecular features and showcase how contingent evolutionary novelties might shape ecologically important microbial innovations.

Acute myeloid leukemia (AML) is a rare and aggressive hematologic malignancy. AML progresses rapidly and is indicated by an excess of immature white blood cells. It is caused by high mutational burden over the span of a person’s life. One signature mutated gene includes the tumor suppressor gene TP53. Normally, TP53 helps make protein to stop oncogenesis or the formation of tumors. However, mutated TP53 loses that function and commonly results in AML. Unfortunately, those that have a TP53 mutation have an extremely aggressive tumor that is resistant to conventional chemotherapy drugs and results in poor prognosis. Other standard treatments include stem-cells transplants, and sometimes targeted drugs such as intracellular pathway inhibitors. Although many treatments are routine and help the patient reduce symptoms, there is no cure. Extensive research is currently being done by researchers and physicians to identify new approaches for AML treatment.

One novel therapy used in other hematologic malignancies includes chimeric antigen receptor (CAR)-T cell therapy. This therapy takes immune T cells (responsible for lysing or kill infections) from the patient or a donor and engineers them to target the tumor. Normally, these T cells would not recognize tumor growth, therefore, the engineered CAR-T cells are programmed to elicit an immune response and recognize surface markers on the tumor to lyse it. This therapy has been successful in other leukemias such as B-cell acute leukemia, and researchers are working to overcome treatment resistant AML using the same approach.

A recent article in EMBO Molecular Medicine, by Drs. Markus Manz, Stephen Boettcher and others, demonstrate that TP53-mutated AML is resistant to CAR-T cell therapy as a single agent, but can be overcome through combination therapy. Manz and Boettcher are principal investigators from the University of Zurich and the Department of Medical Oncology and Hematology at the University Hospital Zurich (USZ) and focus on mechanisms surrounding hematological diseases. The Zurich team first reported why TP53-mutated AML is resistant to CAR-T cell therapy. Using various models, it was noted that the engineered T cells quickly become ‘exhausted’ or inactive due to overstimulation or surrounding stimuli. The team further studied the underlying mechanism in this disease by concluding that TP53-deficient cells caused resistance through several metabolic pathways. Moreover, these pathways including the mevalonate and Wnt pathways were identified to improve therapeutic efficacy.

Solar eruptions are sending a stream of particles towards Earth, creating spectacular auroras in both hemispheres.

The aurora borealis – in the northern hemisphere – will be potentially visible on Monday night in the US as far south as the midwest. The northern lights, more commonly seen within the Arctic Circle, could also be visible in Scotland.

Odysseus, which was built by Houston-based company Intuitive Machines, powered down one week after landing as lunar night began for 14 days. Flight controllers ordered the spacecraft to snooze for three weeks, while the moon’s south pole faced away from the sun, but they hoped Odie would reawaken once sunlight hit its solar panels again.

“Intuitive Machines started listening for Odie’s wake-up signal on March 20, when we projected enough sunlight would potentially charge the lander’s power system and turn on its radio,” representatives of the company wrote on X, formerly called Twitter.

“For the first time we have shown that even a tiny fraction of cellular material could be identified by a mass spectrometer onboard a spacecraft,” said Dr. Fabian Klenner.


How will we find life on Jupiter’s icy moon, Europa, and Saturn’s icy moon, Enceladus? This is what a recent study published in Science Advances hopes to address as a team of international researchers investigate how ice grains that are discharged from the active plumes of these small moons could possess enough organic material for life to exist. This study holds the potential to help astrobiologists develop the necessary instruments and methods to find life on these small moons, specifically with NASA’s Europa Clipper scheduled to launch this October, whose goal will be to investigate Europa’s habitability potential.

Artist’s illustration of Saturn’s moon, Enceladus, seen here upside down as the plumes are on the south pole. (Credit: NASA/JPL-Caltech)

Image of Jupiter’s moon, Europa, obtained in natural light by NASA’s Juno spacecraft. (Credit: NASA/JPL-Caltech/SwRI/MSSS/Kevin M. Gill)

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