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Real-world social cognition requires processing and adapting to multiple dynamic information streams. Interpreting neural activity in such ecological conditions remains a key challenge for neuroscience. This study leverages advancements in de-noising techniques and multivariate modeling to extract interpretable EEG signals from pairs of participants (male-male, female-female, and male-female) engaged in spontaneous dyadic dance. Using multivariate temporal response functions (mTRFs), we investigated how music acoustics, self-generated kinematics, other-generated kinematics, and social coordination uniquely contributed to EEG activity. Electromyogram recordings from ocular, face, and neck muscles were also modeled to control for artifacts. The mTRFs effectively disentangled neural signals associated with four processes: (I) auditory tracking of music, (II) control of self-generated movements, (III) visual monitoring of partner movements, and (IV) visual tracking of social coordination. We show that the first three neural signals are driven by event-related potentials: the P50-N100-P200 triggered by acoustic events, the central lateralized movement-related cortical potentials triggered by movement initiation, and the occipital N170 triggered by movement observation. Notably, the (previously unknown) neural marker of social coordination encodes the spatiotemporal alignment between dancers, surpassing the encoding of self-or partner-related kinematics taken alone. This marker emerges when partners can see each other, exhibits a topographical distribution over occipital areas, and is specifically driven by movement observation rather than initiation. Using data-driven kinematic decomposition, we further show that vertical bounce movements best drive observers’ EEG activity. These findings highlight the potential of real-world neuroimaging, combined with multivariate modeling, to uncover the mechanisms underlying complex yet natural social behaviors.

Significance statement Real-world brain function involves integrating multiple information streams simultaneously. However, due to a shortfall of computational methods, laboratory-based neuroscience often examines neural processes in isolation. Using multivariate modeling of EEG data from pairs of participants freely dancing to music, we demonstrate that it is possible to tease apart physiologically established neural processes associated with music perception, motor control, and observation of a partner’s movement. Crucially, we identify a previously unknown neural marker of social coordination that encodes the spatiotemporal alignment between dancers, beyond self-or partner-related kinematics alone. These findings highlight the potential of computational neuroscience to uncover the biological mechanisms underlying real-world social and motor behaviors, advancing our understanding of how the brain supports dynamic and interactive activities.

Controlling the uniformity in size and quantity of macroscopic three-dimensional (3D) DNA crystals is essential for their integration into complex systems and broader applications. However, achieving such control remains a major challenge in DNA nanotechnology. Here, we present a novel strategy for synthesizing monodisperse 3D DNA single crystals using microfluidic double-emulsion droplets as nanoliter-scale microreactors. These uniformly sized droplets can shrink and swell without leaking their inner contents, allowing the concentration of the DNA solution inside to be adjusted. The confined volume ensures that, once a crystal seed forms, it rapidly consumes the available DNA material, preventing the formation of additional crystals within the same droplet. This approach enables precise control over crystal growth, resulting in a yield of one DNA single crystal per droplet, with a success rate of up to 98.6% ± 0.9%. The resulting DNA crystals exhibit controlled sizes, ranging from 19.3 ± 0.9 μm to 56.8 ± 2.6 μm. Moreover, this method can be applied to the controlled growth of various types of DNA crystals. Our study provides a new pathway for DNA crystal self-assembly and microengineering.

After more than five decades of mystery, scientists have finally unveiled the detailed structure and function of a long-theorized molecular machine in our mitochondria — the mitochondrial pyruvate carrier.

This microscopic gatekeeper controls how cells fuel themselves by transporting pyruvate, a key energy source, across mitochondrial membranes. Now visualized using cryo-electron microscopy, the carrier’s lock-like mechanism could be the key to tackling diseases like cancer, diabetes, and even hair loss. By blocking or modifying this gateway, researchers believe we could reroute how cells generate energy and develop powerful, targeted treatments.

Unlocking a Mitochondrial Mystery.

It’s no wonder engineers have long dreamed of harnessing these powers in human-made structures. Now, scientists have combined fungus and bacteria to create a living material that stays alive for up to a month and can form bone-like structures. The researchers say this approach could one day be used to create structural components that repair themselves.

“We are excited about our results and look forward to engineering more complex and larger structures,” Chelsea Heveran at Montana State University, who led the study, told New Scientist. “When viability is sufficiently high, we could start really imparting lasting biological characteristics to the material that we care about, such as self-healing, sensing, or environmental remediation.”

Researchers have long studied quantum entanglement to understand how photons appear to influence each other instantaneously.

This peculiar link first emerged when Albert Einstein pointed to what he called “spooky action at a distance,” suggesting that this peculiar behavior contradicted intuitive views of cause and effect.

The conversation around these phenomena has evolved through the decades.

Measles, a highly contagious viral infection, continues to pose a significant public health threat worldwide. Despite the availability of effective vaccines, outbreaks persist, particularly in regions with low immunization rates. In 2023, the World Health Organization observed up to a 30-fold increase in measles cases in Europe. There are currently no treatment options for measles. Instead, patients must allow the virus to take its course and let the immune system naturally clear the infection.

Erica Ollmann Saphire, a structural biologist, and her research team at the La Jolla Institute for Immunology uncovered the structure of the measles glycoprotein and engineered a neutralizing antibody against it. This therapy could be implemented to manage measles outbreaks worldwide.


Researchers uncovered the structure of the measles fusion glycoprotein and identified a neutralizing antibody capable of decreasing its virulence.