How the cheese-noodle principle could help counter Alzheimer’s

Researchers at the Paul Scherrer Institute PSI have clarified how spermine – a small molecule that regulates many processes in the body’s cells – can guard against diseases such as Alzheimer’s and Parkinson’s: it renders certain proteins harmless by acting a bit like cheese on noodles, making them clump together. This discovery could help combat such diseases. The study has now been published in the journal Nature Communications.

Our life expectancy keeps rising – and as it does, age-related illnesses, including neurodegenerative diseases such as Alzheimer’s and Parkinson’s, become increasingly common. These diseases are caused by accumulations in the brain of harmful protein structures consisting of incorrectly folded amyloid proteins. Their shape is reminiscent of fibres or spaghetti. To date, there is no effective therapy to prevent or eliminate such accumulations.

Yet a naturally occurring molecule in the body called spermine offers hope. In experiments, researchers led by study leader Jinghui Luo, in the Center for Life Sciences at the Paul Scherrer Institute PSI, have discovered that this substance is capable of extending the life span of small nematode worms, improving their mobility in old age, and strengthening the powerhouses of their cells – the mitochondria. Specifically, the researchers observed how spermine helps the body’s immune system eliminate nerve-damaging accumulations of amyloid proteins. 

The new findings could serve as a basis for developing novel therapies for such diseases.

A central mediator of cellular processes

Spermine is a vital substance for the organism. It belongs to the so-called polyamines, which are relatively small organic molecules. Spermine, first discovered more than 150 years ago, is named after the seminal fluid, as it is found in particularly high concentrations there. But it also occurs in many other cells of the body – especially those that are active and capable of dividing.

Spermine promotes cell mobility and activity and controls numerous processes. Above all, it interacts with the nucleic acids of the genome, regulating the expression of genes and their conversion into proteins. This ensures that cells can properly grow and divide and ultimately die. Spermine is also central to an important cellular process called biomolecular condensation: In this process, certain macromolecules, such as proteins and nucleic acids, segregate and collect within the cell in a droplet-like form, so that important reactions can take place there.

In connection with neurodegenerative diseases such as Alzheimer’s or Parkinson’s, there has previously been evidence that spermine can protect nerve cells and alleviate age-related memory loss. Lacking until now, however, has been a more precise understanding of how spermine intervenes in nerve-damaging processes – understanding that might make it possible to derive medical benefits from it.

Assisting cellular waste removal

Jinghui Luo’s group has now investigated this in more detail. In addition to optical microscopy, the researchers also used the SAXS scattering technique at PSI’s Swiss Light Source SLS to shed light on the molecular dynamics of these processes. The investigations were conducted both in a glass capillary (in vitro) and in a living organism (in vivo). The nematode C. elegans served as a model organism.

Read more on the PSI website

Image: Jinghui Luo is a researcher at the Center for Life Sciences at the Paul Scherrer Institute PSI. He studies accumulations of so-called amyloid proteins, which lead to nerve damage in the brain. His research aims to help mitigate neurodegenerative diseases such as Alzheimer’s and Parkinson’s in the long term.

Credit: © Paul Scherrer Institute PSI/Markus Fischer

A new approach allows researchers to catch a photocatalyst in action

Using SLAC’s X-ray laser, the method revealed atomic motions in a simple catalyst, opening the door to study more complex molecules key to chemical processes in industry and nature.

Catalysts facilitate crucial chemical reactions in nature and industry alike. In a subset of them, catalytic activity is triggered by light. For example, when iron pentacarbonyl – a molecule in which a central iron atom is surrounded by five carbon monoxide groups – is exposed to light, the iron sheds its carbon monoxide groups one after another, creating spots for other molecules to dock on to during a catalytic reaction.  

Although this process has been studied extensively with spectroscopy, a method that shows how energy moves around in molecules, key details of how the catalyst’s atoms change structure after being hit by light remain unknown. 

Now, writing in the journal Nature Communications, a team led by researchers at the Department of Energy’s SLAC National Accelerator Laboratory report how they used ultrafast X-rays from the Linac Coherent Light Source (LCLS), combined with recent theoretical advancements, to reveal those atomic motions on a timescale of femtoseconds, millionths of a billionth of a second. The technique could be used to observe speedy atomic motions in more complex catalysts. 

Understanding how energy flows through molecules and how atoms move in real space and time brings us one step closer to controlling chemical reactions, helping us design materials.Adi NatanSLAC Staff Scientist and Principal Investigator at the Stanford PULSE Institute

“Part of the fun is to make tools that will open new doors,” said Adi Natan, principal investigator and staff scientist at the Stanford PULSE Institute, a joint institute of SLAC and Stanford University. “And being able to see how molecular structures evolve with unprecedented detail will allow us to learn something new about the chemistry of molecules.”

Read more on SLAC website