• University of Cambridge Featured PhD Programmes
  • University of Tasmania Featured PhD Programmes
  • FindA University Ltd Featured PhD Programmes
  • Staffordshire University Featured PhD Programmes
  • Aberdeen University Featured PhD Programmes
  • University of Pennsylvania Featured PhD Programmes
University of Liverpool Featured PhD Programmes
University of Bristol Featured PhD Programmes
Imperial College London Featured PhD Programmes
Imperial College London Featured PhD Programmes
University of Tasmania Featured PhD Programmes

The impact of the the site of translation on the spatial proteome

  • Full or part time
    Prof Kathryn Lilley
  • Application Deadline
    Applications accepted all year round
  • Awaiting Funding Decision/Possible External Funding
    Awaiting Funding Decision/Possible External Funding

Project Description


Prof. Kathryn Lilley, Department of Biochemistry, University of Cambridge
Prof. Anne Willis, MRC Toxicology Unit, Leicester University (re-locating to Cambridge in 2018)

It is now widely acknowledged that mRNA is spatially organised such that its translation frequently occurs in the vicinity where the corresponding protein product adopts its function. This phenomenon has been studied extensively in specialised cells, however, recent research has suggested that spatial restriction of mRNA storage and translation is much more widespread. Aberrant localised protein synthesis is known be associated with developmental defects, cancers and neurological disorders, therefore understanding underlying mechanisms will be important in developing future therapeutic strategies.

The aims of research in the supervisors’ labs are to define where translation of mRNA takes place in the cell, how this is regulated by protein binding partners and sequence motifs and how this changes upon cellular perturbation.
In this project, which will be based in Cambridge, the PhD candidate will carry out crucial experiments aimed at determining the relationship between the transcriptome and spatial proteome and how this changes upon stimulation with insulin.
The project will involve the use of different protein extraction methods, and characterisation of peptides generated from the cell lysates by cutting edge quantitative proteomics methods and informatics tools. Additional experiments will isolate mRNA species from different subcellular niches and resulting data sets will be integrated to determine if the site of translation correlates with the final location of a protein. The project will involve interaction with Cambridge and Leicester based members of the research groups and presentation of data.
The student will learn quantitative mass spectrometry, protein chemistry, tissue culture, cell imaging, ribosomal profiling and next generation sequencing, plus familiarization with several programming languages and basic statistical skills.


The project will fit at the core of the group research activity of both the Lilley and Willis groups. The student will be supported and assisted by other members of these groups, including bioinformaticians, cell biologists and proteomics experts.

This project fits into the category of World Class Underpinning Bioscience/New Ways of Working

Learning outcomes and skills acquired (maximum 100 words)
The student will become familiar with the field of cell biology, translation , proteomics and mass spectrometry.

The skills acquired will be cell culture, basic protein and RNA biochemistry, next generation DNA sequencing, ribosomal profiling, mass spectrometry, quantitative proteomics approaches including SILAC and isobaric tagging, bioinformatics and data interpretation.

The student will also be expected to give a talk about their short project and will be given training in presentation skills, both oral and written.

The student will be working in two vibrant research groups and will be given the opportunity to work as part of large teams of PhD students and post doctoral research workers.

References

1. A draft map of the mouse pluripotent stem cell spatial proteome Christoforou A, Mulvey CM, Breckels LM, Geladaki A, Hurrell T Hayward PC, Naake T, Gatto L, Viner R, Martinez Arias A and Lilley KS (2016) Nature Communications 12;7:9992. doi: 10.1038/ncomms9992
2. Learning from Heterogeneous Data Sources: An Application in Spatial Proteomics., Breckels LM, Holden SB, Wojnar D, Mulvey CM, Christoforou A, Groen A, Trotter MW, Kohlbacher O, Lilley KS, Gatto L. PLoS Comput Biol. 2016 May 13;12(5):e1004920. doi: 10.1371/journal.pcbi.1004920.

How good is research at University of Cambridge in Biological Sciences?

FTE Category A staff submitted: 189.63

Research output data provided by the Research Excellence Framework (REF)

Click here to see the results for all UK universities

Email Now

Insert previous message below for editing? 
You haven’t included a message. Providing a specific message means universities will take your enquiry more seriously and helps them provide the information you need.
Why not add a message here
* required field
Send a copy to me for my own records.
Email Sent

Share this page:

Cookie Policy    X