22 February 2024

New 3D model: This is how the body’s building blocks are made


Human cells contain ribosomes, a complex machine that produces proteins for the rest of the body. Now the researchers have come closer to understanding how the ribosome works.

Using electron microscopy, scientists have managed to produce a 3D model of a part of the human cell, the ribosome, which is no more than 30 nanometres in diameter. Graphic: Eva Kummer

“It is amazing that we can visualise the atomic details of the ribosome. Because they are tiny – around 20-30 nanometres.”

So says Associate Professor Eva Kummer from the Novo Nordisk Foundation Center for Protein Research, who is responsible for the new study published in Nature Communications.

And don’t worry if you don’t know how much a nanometre is. It is around one billionth of a metre.

Using electron microscopy, Eva Kummer and her colleagues Giang Nguyen and Christina Ritter have managed to produce a 3D model of a part of the human cell, the ribosome, which is no more than 30 nanometres in diameter.

More specifically, they have taken snapshots of how a ribosome is made.

“It is important to understand how the ribosome is built and how it works, because it is the only cell particle that produces proteins in humans and all other living organisms. And without proteins, life would cease to exist,” says Eva Kummer.

Proteins are the primary building blocks of the human body. Your heart, lungs, brain and basically your whole body is made of proteins produced by the ribosome.

“From the outside, the human body looks pretty simple, but then consider the fact that every part of the body consists of millions of molecules, that are extremely complex, and that they all know what to do – that is pretty breathtaking,” says Eva Kummer.

The article continues after the video. 

The complex assembling process of the ribosome. Video: Eva Kummer. 

Folding, assembling, and moving to the right place

Before ribosomes can start to produce proteins, they first need to be assembled from over 80 different components.

Eva Kummer and her colleagues have obtained 3D models of three different stages of ribosome assembly.

“It is a complex particle with lots of different parts – many proteins and RNA components – that must be folded, assembled, and moved to the right place. It does not all happen at once. Ribosome assembly is a gradual process involving several stages,” she explains.

Out of the three stages, the 3D model describing the earliest time point in the assembly is the most interesting, according to Eva Kummer, as no one has been able to describe it before.

“At this stage, we can tell e.g. that a specific protein called GTPBP10 is eager to interact with a so-called RNA component that forms a long helix,” Eva Kummer says and adds:

“In fact, towards the bottom of that helix is the catalytic centre of the ribosome, which is where proteins are made. This is why it is so important that the helix is folded and placed correctly. ”

To achieve this, GTPBP10 grabs the helix and puts it in the right position for protein synthesis.

This is just one of the many stages of ribosome assembly which the new study has shed light on – insight that may pave the way for more knowledge of various diseases.

“Errors in ribosome assembly severely reduce the capacity of our cells to make proteins. These are for example proteins that convert the energy from the food we eat into energy coins that the body can use to run all sorts of cellular processes. Now, if the mitochondrial ribosome does not work, our body cannot produce enough energy coins anymore and this leads to diseases such as neurodegenerative disorders and heart conditions. And during ageing, the production of these energy coins also works less and less efficiently,” Eva Kummer says and adds:

“The first step is understanding how things work. Only then can you try to change them.”

You can read “Structural insights into the role of GTPBP10 in the RNA maturation of the mitoribosome“ in Nature Communications.


Associate Professor Eva Kummer

Journalist og press consultant Liva Polack
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