Abstract
This thesis includes two parts. Part I, ‘Development of a peptide microarray method
to study post-translational modifications’ and part II, ‘Toxicity of galectin-9 toward
KRAS mutated CRC cells: pathway elucidation’. Part I aimed to study the posttranslational modifications (PTMs), O-GlcNAcylation/ de- O-GlcNAcylation,
phosphorylation/ dephosphorylation, crosstalk between de-O-GlcNAcylation
and dephosphorylation and finally O-GlcNAcylation of JAK2 JH1 kinase using
short peptide substrates derived from their parental proteins. Part II of this thesis, ‘Toxicity of galectin-9 toward KRAS mutated CRC cells:
pathway elucidation’, aimed to profile the STK and PTK activity of galectin-9
sensitive DLD-1 cancer cells using peptide microarrays. The goal was to identify
the kinase pathways which are involved upon galectin-9 treatment and includes two
chapters.
| Original language | English |
|---|---|
| Qualification | Doctor of Philosophy |
| Awarding Institution |
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| Supervisors/Advisors |
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| Award date | 15 Mar 2023 |
| Publisher | |
| Print ISBNs | 978-94-6458-883-5 |
| DOIs | |
| Publication status | Published - 15 Mar 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- galectin-9
- RAS/ERK pathway
- Kinase signaling pathway, Kinome profiling
- phosphorylation
- O-GlcNAcylation
- peptide microarray
- OGT
- OGA
- PTMs crosstalk
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