Elucidation of the role of newly discovered post-translational modification of proteins involved in hypoxia signalling using proteomic analysis and live cell imaging


The hypoxia signalling pathway is required for the adaptation of cells to a low oxygen environment, which cells can experience in various physiological and pathological circumstances related to high altitude, development, wound healing and cancer.

Hypoxia inducible factor (HIF) is the main transcription factor involved in the cellular adaptation to hypoxia and it is therefore crucial to understand how HIF and its main partners are regulated. Whilst HIF regulation by hydroxylation has been described for years, no other HIF post-translational modifications (PTMs) triggered by hypoxia has been investigated in an unbiased way, and their impact on binding interactions have not yet been elucidated. We have initiated the elucidation of HIF PTMs using mass spectrometry (MS)-based proteomics strategies.

This project will follow on our initial discoveries by investigating the temporal regulation of HIF PTMS and their specificity to the different HIF family members. In addition to understanding the type and site of protein modification as a function of different O2 levels, state-of-the art MS techniques will be exploited to understand how these PTMs occur in combination (at the level of the intact protein). Importantly, the student will have an exciting opportunity of testing the relevance of the major PTMs discovered using live-cell imaging experiments by expressing PTM mimetic and ‘dead’ mutants of HIF, tagged with fluorescent proteins.

The imaging approach will be used to test HIF dynamics and binding to partners at single cell and single molecule level. The student will work and will be trained both in the world class Centre for Proteome Research, within a group working at the forefront of protein modifications analysis, and the Centre for Cell Imaging.

The project is suited to a student with at least a good B.Sc. Upper Second in Biological or Life Sciences, with a solid knowledge in biochemistry and cell signalling.

This psotion will close once a suitable candidate is found, Early applications are encouraged.

To apply please click here


Open to students worldwide

Funding information

Self-funded project

The project is open to both European/UK and International students. It is UNFUNDED and applicants are encouraged to contact the Principal Supervisor directly to discuss their application and the project.

Assistance will be given to applications who are applying to international funding schemes.

The successful applicant will be expected to provide the funding for tuition fees and living expenses as well as research costs of £5,000 per year.

A fee bursary may be available for well qualified and motivated applicants.

Details of costs can be found on the University website



Taylor, S. E., Bagnall, J., Mason, D., Levy, R., Fernig, D. G., and See, V. (2016) Differential sub-nuclear distribution of hypoxia-inducible factors (HIF)-1 and -2 alpha impacts on their stability and mobility. Open Biol 6;

Bagnall, J., Leedale, J., Taylor, S. E., Spiller, D. G., White, M. R., Sharkey, K. J., Bearon, R. N., and See, V. (2014) Tight control of hypoxia-inducible factor-alpha transient dynamics is essential for cell survival in hypoxia. J Biol Chem 289, 5549-5564 


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