Z03
Project Area Z - Central Services
Dr. Farnusch Kaschani
Analytics Core Facility Essen (ACE)
Center of Medical Biotechnology (ZMB)
University of Duisburg-Essen
Phone: +49 201 183 4924
Email
Central proteomics support
Mass spectrometry (MS)-based proteomics has evolved into a robust and powerful technology for timely mechanistic molecular biology research and is thus ideally suited to support the investigation of cell state transitions. The Analytics Core Facility Essen (ACE) will provide state-of-the-art high-resolution, label-based or label-free quantitative ‘bottom up’ mass spectrometry-based proteomics as well as the required expertise for sample preparation workflows and data evaluation to all CRC members. This will for example allow to reveal molecular mechanisms regulating cell state transitions by identifying and dissecting protein-protein interactions (using label-free quantification strategies, proximity labelling or crosslinking MS) and characterizing dynamic changes in expression levels or post-translational modification (PTM) patterns in isolates or whole proteomes.
Project Members
Dr. Sabrina Ninck
Publications
-
Conformational plasticity of a BiP-GRP94 chaperone complexIn: Nature Structural & Molecular Biology, Vol. 32, 2025, Nr. 10, pp. 1947 – 1958DOI (Open Access)
-
Small Molecule-Induced Alterations of Protein Polyubiquitination Revealed by Mass-Spectrometric Ubiquitome AnalysisIn: Angewandte Chemie International Edition, Vol. 64, 2025, Nr. 32, e202508916DOI (Open Access)
-
Sulphostin-inspired N-phosphonopiperidones as selective covalent DPP8 and DPP9 inhibitorsIn: Nature Communications, Vol. 16, 2025, Nr. 1, 3208DOI (Open Access)
-
High resolution analysis of proteolytic substrate processingIn: The Journal of Biological Chemistry (JBC), Vol. 300, 2024, Nr. 11, 107812DOI, Online Full Text (Open Access)
-
Induced degradation of SNAP-fusion proteinsIn: RSC Chemical Biology, Vol. 5, 2024, Nr. 12, pp. 1232 – 1247DOI (Open Access)
-
Microtubule end-on attachment maturation regulates Mps1 association with its kinetochore receptorIn: Current Biology, Vol. 34, 2024, Nr. 11, pp. 2279 – 2293.e6DOI (Open Access)
-
TopBP1 utilises a bipartite GINS binding mode to support genome replicationIn: Nature Communications, Vol. 15, 2024, Nr. 1, 1797DOI, Online Full Text (Open Access)
-
Clp-targeting BacPROTACs impair mycobacterial proteostasis and survivalIn: Cell, Vol. 186, 2023, Nr. 10, pp. 2176 – 2192.e22DOI (Open Access)
-
Structure of the peroxisomal Pex1/Pex6 ATPase complex bound to a substrateIn: Nature Communications, Vol. 14, 2023, Nr. 1, 5942DOI (Open Access)
-
The UBX domain in UBXD1 organizes ubiquitin binding at the C-terminus of the VCP/p97 AAA-ATPaseIn: Nature Communications, Vol. 14, 2023, Nr. 1, 3258DOI, Online Full Text (Open Access)
-
Persister state-directed transitioning and vulnerability in melanoma
32. Deutscher Hautkrebskongress (ADO-Jahrestagung), 14.–17. September 2022, Hannover, Germany,In: Nature Communications, Vol. 13, 2022, Nr. 1, pp. 35 – 36DOI, Online Full Text (Open Access) -
Statins affect cancer cell plasticity with distinct consequences for tumor progression and metastasisIn: Cell Reports, Vol. 37, 2021, Nr. 8, 110056DOI, Online Full Text (Open Access)
-
Redirecting resistance evolution in BRAFV600 melanoma by inhibition of the peroxiredoxin-thioredoxin system2025DOI (Open Access)
-
Targeted degradation of USP7 in solid cancer cells reveals disparate effects of deubiquitinase inhibition vs. acute protein depletion2025DOI, Online Full Text (Open Access)
-
A non-autonomous protein quality control mechanism targeting tau aggregate propagation2024DOI (Open Access)
-
Ipl1-controlled attachment maturation regulates Mps1 association with its kinetochore receptor2023DOI (Open Access)