Sophie Verrier

ORCID: 0000-0003-1308-5229
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About
Contact & Profiles
Research Areas
  • Cellular transport and secretion
  • Lipid Membrane Structure and Behavior
  • Advanced Fluorescence Microscopy Techniques
  • Photoreceptor and optogenetics research
  • Cytokine Signaling Pathways and Interactions
  • ATP Synthase and ATPases Research
  • Advanced biosensing and bioanalysis techniques
  • Pancreatic function and diabetes
  • Endoplasmic Reticulum Stress and Disease
  • Retinal Development and Disorders
  • Protein Tyrosine Phosphatases
  • Blood disorders and treatments
  • Immunodeficiency and Autoimmune Disorders
  • Galectins and Cancer Biology
  • Extracellular vesicles in disease
  • Photosynthetic Processes and Mechanisms

Max Planck Institute for Biophysical Chemistry
2003-2017

Max Planck Society
2005-2008

Presynaptic active zones (AZs) are unique subcellular structures at neuronal synapses, which contain a network of specific proteins that control synaptic vesicle (SV) tethering, priming, and fusion. Munc13s core AZ with an essential function in SV priming. In hippocampal neurons, two different Munc13s-Munc13-1 bMunc13-2-mediate opposite forms presynaptic short-term plasticity thus differentially affect characteristics. We found most presynapses cortical neurons only Munc13-1, whereas ∼10%...

10.1083/jcb.201606086 article EN cc-by-nc-sa The Journal of Cell Biology 2017-03-06

The adrenoleukodystrophy protein (ALDP) and the 70-kDa peroxisomal membrane (PMP70) are half-ATP-binding cassette (ABC) transporters in mammalian peroxisome membrane. Mutations gene encoding ALDP result a devastating neurodegenerative disorder, X-linked (X-ALD) that is associated with elevated levels of very long chain fatty acids because impaired beta-oxidation. interactions ABC transporters, their role membrane, functions disease pathogenesis poorly understood. Studies on revealed...

10.1074/jbc.m702122200 article EN cc-by Journal of Biological Chemistry 2007-07-04

Adopted for the live cell, methods of fluorescence resonance energy transfer (FRET) together with GFP-technology have taken us beyond limits optical resolution and allow to resolve proteinÐprotein interactions in 3-7 nm proximity real time a cell. To reliably study cellular proteins involved trafficking cholera toxin we first analysed maturation each chimeric protein. Cytosolic partners responsible transport were fused cyan fluorescent protein (CFP) co-expressed yellow (YFP)-fused...

10.1117/12.479842 article EN Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE 2003-07-30
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