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Scientists have discovered a protein that can directly halt DNA damage. Better yet, a new study shows it appears to be ‘plug and play’, theoretically able to slot into any organism, making it a promising candidate for a cancer vaccine.

DNA damage response protein C (DdrC) was found in a hardy little bacterium called Deinococcus radiodurans. DdrC seems to be very effective at detecting DNA damage, putting a stop to it and alerting the cell to start the repair process.

But DdrC’s best feature might be that it’s pretty self-contained, doing its job without the help of other proteins.

A novel method utilising genes in our body to perform long-sequence DNA recombination and editing, called the RNA bridge, has been discovered and reported by genetic engineers. ThePrint #̦PureScience, Sandhya Ramesh explains the findings and implications.

Sources and further reading:

- Bridge RNAs direct programmable recombination of target and donor DNA https://www.nature.com/articles/s4158

- Structural mechanism of bridge RNA-guided recombination https://www.nature.com/articles/s4158

A sweat-powered wearable has the potential to make continuous, personalized health monitoring as effortless as wearing a Band-Aid. Engineers at the University of California San Diego have developed an electronic finger wrap that monitors vital chemical levels—such as glucose, vitamins, and even drugs—present in the same fingertip sweat from which it derives its energy.

The advance was published Sept. 3 in Nature Electronics by the research group of Joseph Wang, a professor in the Aiiso Yufeng Li Family Department of Chemical and Nano Engineering at UC San Diego.

The device, which wraps snugly around the finger, draws power from an unlikely source—the fingertip’s . Fingertips, despite their , are among the body’s most prolific sweat producers, each packed with over a thousand . These glands can produce 100 to 1,000 times more sweat than most other areas of the body, even during rest.

In the rapidly evolving world of 3D printing, the pursuit of faster, more efficient and versatile production methods is never-ending. Traditional 3D printing techniques, while groundbreaking, are often time-consuming and limited in the kinds of materials they can use as feedstock.

But, through a new process a Lawrence Livermore National Laboratory (LLNL) team is calling Microwave Volumetric Additive Manufacturing (MVAM), researchers have introduced an innovative new approach to 3D printing using microwave energy to cure materials, opening the door to a broader range of materials than ever before.

In a recent paper published in Additive Manufacturing Letters, LLNL researchers describe the potential of microwave energy to penetrate a wider range of materials compared to light-based volumetric additive manufacturing (VAM).

Imagine you’re sitting across from a friend, having a conversation.


I’m a die-hard Beach Boys fan. In one of their most famous songs, they sing about “pickin’ up good vibrations” from a girl. We’ve all felt those “good vibes” when we’re connecting with someone new. I used to think that feeling was a mysterious, mystical experience — something I couldn’t fully explain that bonded me with some friends and strangers more easily than others.

It turns out that “good vibes” aren’t as mysterious as I thought.

Pioneering neuroscientists have begun investigating how the brain works when we are interact ing with others — a technique they call hyperscanning. Neuroscientists have been using existing scanning methods, like MRI and EEG, to monitor the brain activity of two or more people as they do something together: for example, performing music, learning a poem, or having a conversation.

This gene therapy treats LCA1, causing early childhood vision loss, affecting under 100,000 people:


“One patient reported for the first time being able to navigate at midnight outdoors only with the light of a bonfire,” said Cideciyan, who is also co-director of the Center for Hereditary Retinal Degenerations.

The clinical trials were co-led by researchers from the Perelman School of Medicine at the University of Pennsylvania.

During the worst days of the COVID-19 pandemic, many of us became accustomed to news reports on the reproduction number R, which is the average number of cases arising from a single infected case. If we were told that R was much greater than 1, that meant the number of infections was growing rapidly, and interventions (such as social distancing and lockdowns) were necessary. But if R was near to 1, then the disease was deemed to be under control and some relaxation of restrictions could be warranted. New mathematical modeling by Kris Parag from Imperial College London shows limitations to using R or a related growth rate parameter for assessing the “controllability” of an epidemic [1]. As an alternative strategy, Parag suggests a framework based on treating an epidemic as a positive feedback loop. The model produces two new controllability parameters that describe how far a disease outbreak is from a stable condition, which is one with feedback that doesn’t lead to growth.

Parag’s starting point is the classical mathematical description of how an epidemic evolves in time in terms of the reproduction number R. This approach is called the renewal model and has been widely used for infectious diseases such as COVID-19, SARS, influenza, Ebola, and measles. In this model, new infections are determined by past infections through a mathematical function called the generation-time distribution, which describes how long it takes for someone to infect someone else. Parag departs from this traditional approach by using a kind of Fourier transform, called a Laplace transform, to convert the generation-time distribution into periodic functions that define the number of the infections. The Laplace transform is commonly adopted in control theory, a field of engineering that deals with the control of machines and other dynamical systems by treating them as feedback loops.

The first outcome of applying the Laplace transform to epidemic systems is that it defines a so-called transfer function that maps input cases (such as infected travelers) onto output infections by means of a closed feedback loop. Control measures (such as quarantines and mask requirements) aim to disrupt this loop by acting as a kind of “friction” force. The framework yields two new parameters that naturally describe the controllability of the system: the gain margin and the delay margin. The gain margin quantifies how much infections must be scaled by interventions to stabilize the epidemic (where stability is defined by R = 1). The delay margin is related to how long one can wait to implement an intervention. If, for example, the gain margin is 2 and the delay margin is 7 days, then the epidemic is stable provided that the number of infections doesn’t double and that control measures are applied within a week.