A strategy to kill cancer cells by inducing proteotoxic stress

PhD

In Dundee

Price on request

Description

  • Type

    PhD

  • Location

    Dundee (Scotland)

  • Duration

    Flexible

  • Start date

    Different dates available

Cancer cells are heavily reliant on their ubiquitin proteasome system (UPS) to maintain proteostasis and cell survival. This is because cancer genomes have many mutations in protein coding sequence, deletions, translocations as well as copy number variations. This results in the expression of mutant proteins and disruption of stoichiometric complexes, which have to be degraded. Moreover, malignant cells have high rates of proliferation and protein synthesis. Thus, cancer cells are dependent on protein quality control systems for survival. The available projects build on the Kulathu lab’s main interests in understanding how protein degradation and proteostasis are modulated by the ubiquitin system.

Facilities

Location

Start date

Dundee (Dundee City)
See map
Fulton Building, DD1 4HN

Start date

Different dates availableEnrolment now open

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Reviews

This centre's achievements

2019

All courses are up to date

The average rating is higher than 3.7

More than 50 reviews in the last 12 months

This centre has featured on Emagister for 14 years

Subjects

  • Oncogenic
  • Cancer cells
  • Proteasome
  • Proteasome system
  • Cell survival
  • Cancer genomes
  • Translocations
  • Variations
  • CRISPR
  • Engineering
  • Proteins

Course programme

The overall aims of the projects in this area will be to get a detailed understanding of how ubiquitylation regulates the stability and degradation of oncogenic proteins and how strategies can be designed to modulate them. Specifically, we are interested in exploring a newly identified pathway in the lab that disrupts protein degradation, thus inducing proteotoxic stress. In this project, you will determine how this pathway works and develop strategies to modulate this pathway in cancer cells. During this project, you will have opportunities to learn and apply a wide range of cell biological methods including CRISPR/Cas9 genome engineering, proximity-labelling based identification of interacting proteins, proteomics, high-resolution microscopy, live cell imaging and access to mouse models.

At the MRC PPU, as well as the possibility of a PhD in one particular lab, we offer the possibility of two 4.5-month rotations in labs of their choice. A range of other projects from MRC PPU scientists are advertised on this website. Rotations provide valuable experience and help with deciding on the choice of PhD project and research group.

A strategy to kill cancer cells by inducing proteotoxic stress

Price on request