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We analyzed the interactome of the kinase ERK5 and its mutant Y733E in HeLa cells.
ORGANISM(S): Homo sapiens (Human) 
2020-01-31 | PXD014028 | Pride
Oesophageal adenocarcinoma (OAC) is a deadly disease with poor survival statistics and few targeted therapies available. One of the most common molecular aberrations in OAC is amplification or activation of the receptor tyrosine kinase ERBB2, and ERBB2 is targeted in the clinic for this subset of pa...
ORGANISM(S): Homo sapiens (Human) 
2023-01-03 | PXD029180 | Pride
We developed Proximal Phosphoproteomics Approaches (PPAs)to study RTK endocytosis-dependent proximal signaling in breast cancer cells.
ORGANISM(S): Homo sapiens (Human) 
2021-04-23 | PXD018184 | Pride
We studied Receptor Tyrosine Kinase signalling from recycling endosomes and how this affected downstream responses.
ORGANISM(S): Homo sapiens (Human) 
2022-11-08 | PXD028330 | Pride
We studied Receptor Tyrosine Kinase signalling from recycling endosomes and how this affected downstream responses. We developed a new method to study signalling in the proximity of recycling endosomes by combining enrichment of biotinylated peptides followed by enrichment of phosphorylated peptides...
ORGANISM(S): Homo sapiens (Human) 
2022-11-08 | PXD028371 | Pride
Enhanced fatty acid (FA) synthesis and uptake underpin the sustained membrane biogenesis and ATP production required for melanoma cell growth and division1-4. However, to thrive, melanoma cells must avoid a potential reduction in cell growth signalling, rampant reactive oxygen species (ROS) generati...
ORGANISM(S): Homo sapiens (Human) 
2023-03-10 | PXD017487 | Pride
We studied Receptor Tyrosine Kinase signalling from recycling endosomes and how this affected downstream responses.
ORGANISM(S): Homo sapiens (Human) 
2022-11-08 | PXD028370 | Pride
In this study, we systematically assessed the fine-tuning of limited proteolysis in the extracellular space by glycosylation, one of the most widely observed PTMs, using cells, and applying the Terminal Amine Labeling of Substrates (TAILS) approach, a quantitative proteomics workflow for the system-...
ORGANISM(S): Homo sapiens (Human) 
2024-08-10 | PXD050581 | Pride
In this study, we systematically assessed the fine-tuning of limited proteolysis in the extracellular space by glycosylation, one of the most widely observed PTMs, using cells, and applying the Terminal Amine Labeling of Substrates (TAILS) approach, a quantitative proteomics workflow for the system-...
ORGANISM(S): Homo sapiens (Human) 
2024-08-10 | PXD050647 | Pride
In this study, we systematically assessed the fine-tuning of limited proteolysis in the extracellular space by glycosylation, one of the most widely observed PTMs, using cells, and applying the Terminal Amine Labeling of Substrates (TAILS) approach, a quantitative proteomics workflow for the system-...
ORGANISM(S): Homo sapiens (Human) 
2024-08-10 | PXD050580 | Pride
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