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21.10.2022 17:00

Prions induce toxic Huntingtin oligomers

Dr. Christiane Menzfeld Öffentlichkeitsarbeit
Max-Planck-Institut für Biochemie

    Martinsried. Researchers discovered that prions, which are naturally occurring protein clumps in yeast, are involved in the toxicity of the disease-related protein Huntingtin. They found that the actual toxic form of the Huntingtin protein is not large aggregates, as previously suspected, but smaller intermediates, so-called oligomers. Those intermediates arise through specific interactions with prions. The researchers now suspect similar relationships in human disease. The study was published in the journal Molecular Cell and is an achievement of the team led by Ulrich Hartl at the Max Planck Institute of Biochemistry (MPIB).

    Neurodegenerative diseases like Alzheimer’s, Parkinson’s or Huntington’s disease are characterized by the deposition of protein clumps, so-called protein aggregates, in the brains of patients. Even though disease-relevant proteins – such as the Huntingtin protein in Huntington’s disease – are present in all cells of the human brain, aggregates of Huntingtin form in a specific region of the brain during the initial stage of the disease. A recent study by the group of Ulrich Hartl from the Max Planck Institute of Biochemistry investigates the influence, that the cell type has on this preference of aggregate formation in a distinct brain region. The study has been published in the scientific journal Molecular Cell. To address this phenomenon, the researchers performed experiments in a yeast model system.

    Artificial protein aggregation through blue light illumination
    Similar to the human brain, the formation of Huntingtin aggregates in yeast also depend on the cell type, the so-called yeast strain. While the Huntingtin protein forms aggregates in some yeast strains, it remains soluble in others. Why this is the case hasn’t been understood so far. To investigate the distinction between different yeast strains and how they contribute to the formation of Huntingtin aggregates, the researchers utilized recent advances in the field of optogenetics. They biotechnologically manipulated yeast strains that normally do not allow the aggregation of Huntingtin and integrated a molecular switch that could be activated with blue light. This way, Huntingtin aggregates could be formed simply by illuminating the cells with blue light.

    Comparing the yeast cells that naturally form Huntingtin aggregates with those, that only do so after their activation with blue light, caught the researchers by surprise. Only in cells where Huntingtin aggregates already form naturally, but not in those where the aggregation of Huntingtin was artificially induced with blue light, were toxic effects observed. The first author of the study, Michael Gropp, reasoned that this phenomenon came about because smaller intermediates, rather than large aggregates, are the actual toxic version of the protein. Only in yeast cells that form Huntingtin aggregates naturally, do these smaller toxic intermediates, the oligomers, exist. Here, large aggregates arise slowly, through the accumulation of proteins around the smaller intermediates. These small intermediates are bypassed when the aggregation of Huntingtin is induced artificially with blue light. Large aggregates then appear much more rapidly, avoiding toxic effects.

    The role of prions during aggregate formation
    But why do some yeast strains form Huntingtin aggregates, while other genetically identical strains do not? Further assays in yeast and experiments with purified proteins – proteins that were artificially enriched in a test tube – helped the researchers to understand this phenomenon. Some yeast strains naturally contain protein aggregates of certain proteins, the prions. These prion aggregates are not harmful for the cells. However, due to their specific structure, these prion aggregates can influence soluble Huntingtin proteins and impose their structure on them. As a result, soluble Huntingtin proteins convert into an aggregated state. A side effect of this process is the appearance of toxic intermediates. Yeast strains that naturally do not form Huntingtin aggregates also do not possess prions and are therefore unable to generate toxic intermediates, despite the artificial induction of large Huntingtin aggregates with blue light.

    Possible implications for human disease
    In recent years, many human proteins have been characterized that share similarities with the prions in yeast. A bioinformatic analysis of previously published data sets from mouse models and human cell cultures showed that mammalian proteins with such prion-like characteristics preferentially accumulate in neurons. With the increasing age of an individual, they tend to form aggregates. The authors of the study suspect that the aggregates of these prion-like proteins can in turn force the aggregation of disease-relevant proteins, such as Huntingtin, in certain brain areas and thus contribute to the disease progression in neurodegenerative disorders. Further investigation of this hypothesis is still ongoing.


    Wissenschaftliche Ansprechpartner:

    Prof. Dr. F. Ulrich Hartl
    Department Cellular Biochemistry
    Max Planck Institute of Biochemistry
    uhartl@biochem.mpg.de


    Originalpublikation:

    M. H. M. Gropp, C. L. Klaips and F. U. Hartl: Formation of toxic oligomers of polyQ-expanded huntingtin by prion-mediated cross-seeding, October 2022
    DOI: 10.1016/j.molcel.2022.09.031


    Bilder

    Illustration of yeast cells during the illumination with blue light
    Illustration of yeast cells during the illumination with blue light

    Illustration: Kateryna_Kon, AdobeStock


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    Illustration of yeast cells during the illumination with blue light


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