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A recent groundbreaking discovery identified a novel, copper-dependent form of regulated cell deathcuproptosischaracterized by lipoylated protein aggregation and loss of iron-sulfur clusters

Using HD mouse and cell models, we demonstrated that TFEB and TFE3 are sequestered in muHTT aggregates, and muHTT proteins associates with LMP triggering the translocation of LGALS3 to the lumen of lysosomes, with a close relation between polyQ size and severity of these events

Martin Kampmann explores our current understanding of the cellular and molecular mechanisms that lead to selective vulnerability in different diseases.

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