Akane Kawamura

Photo of Akane Kawamura

Professor Akane Kawamura

Associate Professor and Senior Research Fellow

 

 

Research Interests

The group’s research focuses on understanding the molecular mechanisms of biological processes. We employ a variety of biochemical, biophysical and cell-based functional studies of proteins, alongside development of novel cyclic peptide and small molecule based chemical tools. We have a particular interest in proteins that regulate epigenetic modifications on histones and DNA, and our work seeks to improve understanding of their mechanisms and how they influence the expression of genes. We also tackle challenging protein-protein interactions of biomedical importance, including chemokine signalling and inflammation. We work at the interface of chemistry, biology and medicine, and many of our projects are highly collaborative.

Areas of Interest

 

Chemical Epigenetics 

Epigenetic modifications refer to the covalent modifications to DNA and histones which constitute a set of inherited changes in gene expression, without changing the underlying DNA sequences. By having a molecular understanding and developing chemical probes against the proteins that regulate these epigenetic modifications, we hope to gain a better understanding of epigenetic mechanisms and how they influence the expression of genes in health and disease.

Histone modifiers: Abnormal histone post-translational modification (PTM) patterns and dysregulation of epigenetic enzymes are implicated in many diseases, including cancer.  We study families of epigenetic enzymes that are ‘erasers’ and ‘writers’ of histone PTMs (e.g. histone demethylases (KDM) and methyltransferases). Many of these proteins also contain ‘reader’ domains (e.g. PHD-fingers) which allow them to recognise specific epigenetic marks. Our work has led to the development of new assay platforms, new functional and mechanistic insights into epigenetic enzymes and proteins, factors affecting epigenetic regulation (e.g. O2, (onco)metabolite levels) as well as generation of chemical tools/probes. 

Current projects include: Biochemical and cellular studies of histone demethylases; Investigating the inter-domain and combinatorial PTM cross-talk; Molecular recognition of PTMs by epigenetic proteins; Chemical probe development for epigenetic proteins including KDMs and PHD-finger domains 

DNA Modifiers: Cytosine methylation is established by DNA methyltransferases (DNMTs) and is an important epigenetic mark that regulate gene expression. We study a family of 2OG oxygenases called Ten-Eleven Translocation enzymes (or TETs) which play a key role in the cytosine modification cycle by oxidising methylated cytosines. We have developed activity- and binding-based biochemical assays to study these enzymes. We have also identified potent TET cyclic peptide inhibitors and are working to develop chemical probes which would enable biological role investigations in a cellular context.

Inflammation

Inflammation processes are at the core of many pathologies including several major cardiovascular diseases such as myocarditis, atherosclerosis, and strokes, and influence the fate and drug resistance of cancer. Therefore, leukocyte mobilisation and actions are responsible for many fatalities worldwide and have been the focus of many pharmaceutical development in the last 50 years. We are working to target the chemotactic cytokine (chemokine) network responsible for the leukocyte tissue infiltration using tick saliva proteins (evasins) and peptides inspired from these proteins.

Peptide Discovery Platform 

We utilise a combination of peptide chemistry and peptide-array / mRNA-display technologies for substrate profiling, protein-protein interaction mapping, as well as to generate highly potent and selective ligands against our targets of interest. Some highlights in this area include: substrate profiling of epigenetic enzymes, development of potent and selective cyclic peptides inhibitors against epigenetic enzymes, affinity-based cyclic peptide probes, and anti-inflammatory peptide discovery. 

 

Biography

Akane Kawamura is an Associate Professor in Chemical Biology.  After obtaining M.Chem and D.Phil degrees at University of Oxford, she spent three years in the biotech sector where she led a number of drug discovery projects across a wide range of therapeutic areas. In 2009 she returned to academia as a postdoctoral researcher with Professor Chris Schofield FRS at University of Oxford and in 2012 established her group in the Department of Chemistry and Radcliffe Department of Medicine as a BHF CRE Senior Research Fellow. She was subsequently awarded a Royal Society Dorothy Hodgkin Fellowship (2013-2018) and ERC Starting (2016-2021) and Consolidator (2021-) grants. In 2019, she became a Chair and Professor of Chemical Biology at Newcastle University and currently holds a joint appointment, with research activities at both universities.  Akane is a Director of Oxford-GSK-Crick Chemical Biology CDT (2018-) and a co-director of Chemistry in Cells PhD Programme (2019-).  Her group’s research focuses on understanding the chemistry of epigenetic regulation, protein-protein interactions and the development of chemical probes and (cyclic) peptide-based target validation approaches.

Publications

Contact

akane.kawamura@chem.ox.ac.uk
01865 275910

Research group

Kawamura Research Group

Other websites

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