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Yusuf Hamied Department of Chemistry

 

Herchel Smith Professor of Medicinal Chemistry

Nucleic acids are fundamental to life. Our research is focused on the chemical biology of nucleic acids, and employs the principles of chemistry and the molecular sciences to address questions of importance in biology and medicine. Projects are inherently interdisciplinary and will provide scope for a diversity of intellectual and experimental approaches that include: organic synthesis, biophysics, molecular and cellular biology and genomics. Our scientific goals are problem-driven, which constantly raises the need to invent new methodology.

 

A major interest is to elucidate and manipulate mechanisms that control the expression of genes (either transcription, or translation). We are particularly interested in the role of non-canonical nucleic acid structures that control gene expression (e.g. G-quadruplexes, micro RNA and RNA structures in the 5' untranslated regions of mRNAs). Our goal is to design and synthesise small organic molecules that target such structures and alter the expression of certain genes of interest. Such small molecule gene regulators are valuable tools to study mechanisms in biology and will also open up new approaches for therapeutics and molecular medicine, particularly for diseases characterized by aberrant expression of certain genes (e.g. various cancers).

Our fundamental science will inevitably create opportunities for translation and commercialisation. One such example was our invention (with Professor David Klenerman) of new DNA sequencing technology ("Solexa sequencing") that was commercialised as a Cambridge University spinout company (now part of Illumina Inc.) and is used routinely for applications in genomics, including human genome sequencing. 

Hear Shankar Balasubramanian discuss some of the group's research.

Watch Professor Balasubramanian discuss his research

Take a tour of the Balasubramanian Lab

Publications

Identification of small molecule inhibitors of the Lin28-mediated blockage of pre-let-7g processing.
HL Lightfoot, EA Miska, S Balasubramanian
– Organic & biomolecular chemistry
(2016)
14,
10208
Retinol and ascorbate drive erasure of Epigenetic memory and enhance reprogramming to naïve pluripotency by complementary mechanisms
TA Hore, F von Meyenn, M Ravichandran, M Bachman, G Ficz, D Oxley, F Santos, S Balasubramanian, TP Jurkowski, W Reik
– Proceedings of the National Academy of Sciences of the United States of America
(2016)
113,
12202
G-quadruplex structures mark human regulatory chromatin.
R Hänsel-Hertsch, D Beraldi, SV Lensing, G Marsico, K Zyner, A Parry, M Di Antonio, J Pike, H Kimura, M Narita, D Tannahill, S Balasubramanian
– Nature Genetics
(2016)
48,
1267
An Epigenetics-Inspired DNA-Based Data Storage System.
C Mayer, GR McInroy, P Murat, P Van Delft, S Balasubramanian
– Angewandte Chemie (International ed. in English)
(2016)
55,
11144
RG4-seq reveals widespread formation of G-quadruplex structures in the human transcriptome
CK Kwok, G Marsico, AB Sahakyan, VS Chambers, S Balasubramanian
– Nature Methods
(2016)
13,
841
DSBCapture: In situ capture and sequencing of DNA breaks
SV Lensing, G Marsico, R Hänsel-Hertsch, EY Lam, D Tannahill, S Balasubramanian
– Nature methods
(2016)
13,
855
Structural Analysis using SHALiPE to Reveal RNA G-Quadruplex Formation in Human Precursor MicroRNA.
CK Kwok, AB Sahakyan, S Balasubramanian
– Angewandte Chemie - International Edition
(2016)
55,
8958
In vivo genome-wide profiling reveals a tissue-specific role for 5-formylcytosine
M Iurlaro, GR McInroy, HE Burgess, W Dean, E-A Raiber, M Bachman, D Beraldi, S Balasubramanian, W Reik
– Genome biology
(2016)
17,
141
Structural Analysis using SHALiPE to Reveal RNA G‐Quadruplex Formation in Human Precursor MicroRNA
CK Kwok, AB Sahakyan, S Balasubramanian
– Angewandte Chemie
(2016)
128,
9104
Long genes and genes with multiple splice variants are enriched in pathways linked to cancer and other multigenic diseases
AB Sahakyan, S Balasubramanian
– BMC Genomics
(2016)
17,
225
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Research Group

Research Interest Group

Telephone number

01223 336347

Email address

sb10031@cam.ac.uk