Our Lab
Our research interests are focused on the understanding of the molecular mechanisms which lead to neurodegeneration in diseases such as Parkinson’s, Huntington’s, or Alzheimer’s disease. These diseases are intimately associated with protein misfolding and aggregation in specific regions of the brain.
Because the molecular pathways involved in protein homeostasis are highly conserved, we employ a wide variety of model organisms, from the simple but powerful budding yeast to mammalian cell culture and mice, to study the origin of the problems.
Our ultimate goals are to develop novel therapeutic approaches for these and other related disorders. We are working closely together with clinicians in order to accelerate drug discovery efforts, translating basic research into clinical applications that will improve the lives of patients.
Research Areas
Ph.D positition available (f/m/d)
21.03.2025
Highlights
Heat-Net Meeting 2024
It is our great pleasure to invite you to the our Heat-Net Meeting 2024. Heat-Net Meeting The workshop will be held in September 5-6, 2024, Cádiz https://heatnet2024.uca.es/ [...]
Lecture Dr. Nagendran Ramalingam
Physiological α-synuclein serine-129 phosphorylation is not an oxymoron α-Synuclein is an abundant presynaptic protein that regulates neurotransmission. It is also a key protein implicated in a [...]
A biological classification of Parkinson’s disease: the SynNeurGe research diagnostic criteria
A biological classification of Parkinson's disease: the SynNeurGe research diagnostic criteria With the hope that disease-modifying treatments could target the molecular basis of Parkinson's disease, even before the [...]
Neurodegenerative disorders, including Alzheimer’s disease (AD) and Parkinson ’s disease (PD), affect more than eleven million European citizens, and result in major suffering for patients and [...]
Selected Publications
Exact mechanisms of heat shock–induced lifespan extension, although documented across species, are still not well understood. Here, we show that fully functional peroxisomes, specifically peroxisomal catalase, are needed [...]
Glucocerebrosidase mutations disrupt the lysosome and now the mitochondria
Parkinson’s disease (PD) is a common neurodegenerative condition known for typical motor symptoms associated with the loss of dopaminergic neurons in the substantia nigra. Early genetics studies on [...]
A biological classification of Parkinson’s disease: the SynNeurGe research diagnostic criteria.
With the hope that disease-modifying treatments could target the molecular basis of Parkinson's disease, even before the onset of symptoms, we propose a biologically based classification. Our classification [...]
Chemical synthesis of site-selective advanced glycation end products in α-synuclein and its fragments.
Advanced glycation end products (AGEs) arise from the Maillard reaction between dicarbonyls and proteins, nucleic acids, or specific lipids. Notably, AGEs are linked to aging and implicated in [...]
Stress granules sense metabolic stress at the plasma membrane and potentiate recovery by storing active Pkc1.
As the physical barrier between the cell and the outside environment, the plasma membrane is well-positioned to be the first responder to stress. The membrane is also highly [...]
Translocator protein ligand protects against neurodegeneration in the MPTP mouse model of Parkinsonism.
As the physical barrier between the cell and the outside environment, the plasma membrane is well-positioned to be the first responder to stress. The membrane is also highly [...]