Contact

For any issue, you may contact us at:

Prof. dr. Joost Holthuis (Project Coordinator)

T: +49 541969 7140
F: +49 541969 2498
E: sphingonet@uu.nl

Dr. Matthijs Kol (Project Manager)

T: +49 541 969 7220
F: +49 541969 2498

Renate Sokolowski (Financial Manager)

T: +49 541969 4068
F: +49 541969 4013

 

Recent News

Three Sphingonet partners (EMBL ,UU & UOS) deliver "Hot paper" in Angewandte Chemie:
 Haberkant et al. published the paper "In Vivo Profiling and Visualization of Cellular Protein-Lipid interactions Using Bifunctional Fatty acids" .
The development of this technique paves the way for studying sphingolipid-protein interactions. Research in this direction is ongoing!
 

Recent Events

April 5th, 2013: Approval of progress report year 1
The EU approved our progress report, acknowledging the work progress and achievement of several milestones. This sets the standard for the upcoming reporting events.

Upcoming Events

  • 11 - 13 July  2013, Oxford
    - Summer School, including workshop From Bench to Bedside - Pre-clinical research (Organiser: Frances Platt)
    - Plenary meetings of the Consortium (PIs) and Young Research Council (fellows)
  • 30 September - 4 October 2013, Utrecht
    Mass spectrometry course, definitive program tba
  • (4-6) November 2013, Heidelberg
    Course: photoactivatable proteins and lipids, definitive dates and times tba
  • 7 & 8 November 2013, Heidelberg
    Mid-term review meeting

Fellowships

  • ESR1: “Mapping ceramide homeostatic machinery involved in programmed cell death” [more]
  • ESR2: “Evaluation of sphingolipid homeostatic machinery as target for modulating drug-induced apoptosis in tumors” [more]
  • ESR3: “Identification of cross-talk between sphingolipid and phosphoprotein signaling pathways” [more]
  • ESR4: “Tracing novel mediators of sphingolipid homeostasis using high-throughput visual screens” [more]
  • ESR5: “Tracing novel mediators of sphingolipid homeostasis using toxic peptide reagents” [more]
  • ESR6: “Mechanism of sphingolipid traffic at membrane contact sites” [more]
  • ESR7: “Development and application of semi-synthetic sphingolipid sensors” [more]
  • ESR8: “Generation of peptide ligands to sphingolipids and regulators of sphingolipid homeostasis” [more]
  • ESR9: “Niemann-Pick type C disease: pathogenesis and therapy” [more]
  • ESR10 “Chemical methods to manipulate sphingolipid pools in live cells” [more]
  • ER1: “Development of a novel drug target-profiling platform in yeast” [more]
  • ER2: “Enabling FCCS-based affinity measurements of membrane-drug interactions” [more]

Funded by

  Cordis FP7-People

  Marie Curie Actions

 European Union

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