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Proteostatic stress triggers cristae remodeling and aggregate formation within mitochondria. Credit: Science Advances (2026). DOI: 10.1126/sciadv.aed3579
An international team led by researchers from the University Medical Center Göttingen (UMG), Germany, has used advanced electron microscopy technologies to capture key cellular mechanisms of stress resistance with near-atomic precision. They were able to show that the protein mHsp60, which helps other proteins to adopt their functional form, remodels its structure under stress conditions and thereby increases its activity to ensure mitochondrial functionality.
Their findings may help clarify the processes leading to severe neurodegenerative diseases such as Parkinson's disease. The results are published in the journal Science Advances.
Mitochondria are cellular compartments responsible for producing most of the cell's energy. Consequently, tissues with high energetic demands, such as muscles and the brain, are particularly sensitive to mitochondrial dysfunction. For example, there are specialized nerve cells located primarily in the midbrain that produce and release the neurotransmitter dopamine, the so-called dopaminergic neurons.
Dopamine controls motivation, movement, mood, and drive, therefore they require particularly high amounts of energy. These dopaminergic neurons selectively degenerate in Parkinson's disease, but the underlying mechanisms are not understood. Therefore, no cure exists for this disease, affecting more than 10 million patients worldwide, according to the umbrella organization Parkinson's Europe.
Structural models for mitochondrial remodeling upon proteostatic stress and the mHsp60 functional cycle. Credit: Science Advances (2026). DOI: 10.1126/sciadv.aed3579
One possibility is that the high energy demands of dopaminergic neurons place their mitochondria under extraordinary stress, which may eventually cause these organelles to malfunction.
Conversely, in certain forms of cancer, exacerbated mitochondrial fitness may enhance the proliferative capacity of cancer cells. Therefore, it is crucial to understand the molecular mechanisms that maintain the fine balance of mitochondrial health and stress resistance. However, technological limitations had so far impeded scientists to study these processes at sufficient resolution within cells.
An international team of researchers led by Prof. Dr. Rubén Fernández-Busnadiego, leader of the working group "Structural Cell Biology" at the Department of Neuropathology at the University Medical Center Göttingen (UMG) and member of the Göttingen Cluster of Excellence "Multiscale Bioimaging: From Molecular Machines to Networks of Excitable Cells" (MBExC), have addressed these challenges.
The researchers used an innovative electron microscopy technology known as cryo-electron tomography that enables imaging of three-dimensional (3D) cells frozen by an ultrafast procedure. The advantage: This method preserves the cells in a close-to-native state and shows with near-atomic precision how mitochondria downregulate protein translation and increase protein folding—a crucial process ensuring protein functionality—under stressful conditions in human cells.
In particular, they identified the mitochondrial heat shock protein 60 (mHsp60), an important "folding helper," as a key protein that contributes significantly to mitochondrial functionality under stress conditions.
The researchers were able to show in high resolution how mHsp60 works in general, and how it adapts to stress by remodeling its structure and thereby increasing its activity.
"We carried out a stress test within the cell's energy factories, to analyze the molecular mechanisms of quality control and their weaknesses," says Prof. Fernández-Busnadiego, last author of the study. "We are particularly interested in deciphering the link between cellular stress, protein misfolding and severe neurodegenerative diseases."
Kenneth Ehses, postdoctoral researcher at the Department of Neuropathology at UMG, first author of the study and member of the Hertha-Sponer-College, the MBExC's teaching and training platform, added, "Cryo-electron tomography technology allows us to study protein complexes directly within their native cellular environment, enabling us to investigate possible mechanisms for the development of diseases.
"The findings could contribute to the development of new treatment strategies for neurodegenerative diseases such as Parkinson's disease."
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The study in detail
The team subjected human cells to mitochondrial stress, and subsequently flash-froze them in a close-to-native state at approximately -200 degrees for cryo-electron tomography imaging.
The stress was induced by a chemical substance which causes misfolded and therefore inactive proteins to accumulate in the mitochondria. This triggers an increased formation of mHsp60 complexes, which support other proteins to fold correctly by encapsulating them within a protective barrel-like structure.
Cryo-electron tomography data revealed how these barrels are assembled in human cells, and that the three-dimensional structure of mHsp60 is altered in such a way that it can continue to fold mitochondrial proteins correctly and to an increased extent, even under difficult stress conditions.
Thus, cryo-electron tomography imaging provided sufficient resolution to determine structures of key molecular machines for mitochondrial protein biogenesis, and to analyze their alterations upon stress directly within the cells.
The functional and structural cycle of mHsp60 was analyzed in close collaboration with researchers from the Biofisika Institute in Spain, the Tel Aviv University in Israel and the University of Dundee in the UK. In the next steps, the team will investigate how this cycle is altered under pathological conditions, including Parkinson's disease.
Publication details Kenneth Ehses et al, Structural remodeling of the mitochondrial protein biogenesis machinery under proteostatic stress, Science Advances (2026). DOI: 10.1126/sciadv.aed3579 Journal information: Science Advances
— Source: Phys.org (https://phys.org/news/2026-03-high-resolution-electron-microscopy-cellular.html)
