About us
UCL School of Pharmacy is one of the world's leading centres of excellence for pharmaceutical science, education and professional engagement, ranked third in the world by QS (2025, Pharmacy and Pharmacology). The Division has a track record in high-quality research across a broad range of drug discovery, pharmacy and patient safety-related areas, and for developing spinout companies that have brought new therapeutic strategies to patients.
Further information can be found on our website http://www.ucl.ac.uk/pharmacy/ This is an exciting opportunity to join Professor Zoe Waller's research team.
You will work in a collaborative and innovative team who are committed to understanding i-motif DNA structure and function.
About the role
The main purpose of this position is to use a range of cell biology, molecular biological and biophysical techniques to investigate the stability and biological functions of i-motif DNA secondary structures in human genome and their potential role in the ageing process.
This post will be based in Prof Zoe Waller's lab at UCL School of Pharmacy. The work forms part of a collaborative BBSRC funded grant jointly held with Dr Yiliang Ding (JIC) and Dr Tim Craggs (Sheffield).
The ideal candidate will be a well-trained and highly motivated scientist who will actively drive the research project they will design and conduct experiments under the direction of the PI. They will analyse and present the results, discuss the work with the PI, CoIs and collaborators and be able to communicate the work to both other scientists and the general public. They will be responsible for maintaining accurate records of data and up to date protocols/procedures during the project.
C-rich regions of DNA can form alternative secondary structures called i-motifs, which have not only shown utility as bio-compatible pH-responsive materials in nanotechnology, but also have been shown to exist and act as molecular switches in cells. Although there have been significant advances in this area, we are still yet to understand their prevalence in the human genome and extent of their roles in biology. Our hypothesis is that iM structures form in vivo but natural mutations will affect the function of these structures and could result in age-related diseases and conditions. The project will test this using a range of bioinformatic, biological, biophysical and molecular biology techniques. In this proposal, we will bring together the new understanding of i-motifs to investigate the effects of ageing on these structures, their potential changes in function and how this may play a role in age-related diseases and conditions.
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