Professor of Chemical Biology

Gonçalo Bernardes is a Professor of Chemical Biology & a Fellow of Trinity Hall College, Cambridge.

What we do

Nature has its own machinery for modifying the structure of proteins. In our research, we’re attempting to mimic this machinery to gain significant therapeutic benefits. We’re engineering chemical reactions that enable us to modify proteins while allowing to choose the precise location in the protein’s structure where we want to install these modifications.

This work has a whole range of applications. For example, we’re currently developing ways of selectively labelling proteins in living cells: this can help us monitor the proteins associated with particular diseases without interfering either with the protein’s structure, function, activity and location or upsetting the cell’s normal functions. Another important potential application for this work is linking cytotoxic drug molecules (molecules that are poisonous to cells) to antibodies and then using the antibody to deliver the drug in a very targeted way to the diseased tissue. This could improve the effectiveness of cancer treatments and reduce their side effects.

These are two examples from among our lines of research that use site-selective and bioorthogonal chemistry to address challenges in biology and medicine. We hope our methods may in future be used in laboratories around the world to help develop new drugs with improved effectiveness and reduced side-effects for some of the most common diseases such as cancer.

Funding

We are funded by the Royal Society, by UKRI (EPSRC) and by the European Commission (Marie Sklodowska Curie actions & European Research Council)

For further information on our research and for opportunities, please check our research group website.

Watch Professor Bernardes discuss his research

Take a tour of the Bernardes Lab

Publications

Stable Pyrrole-Linked Bioconjugates through Tetrazine-Triggered Azanorbornadiene Fragmentation
E Gil de Montes, A Istrate, CD Navo, E Jiménez-Moreno, EA Hoyt, F Corzana, I Robina, G Jiménez-Osés, AJ Moreno-Vargas, GJL Bernardes
Angewandte Chemie International Edition
(2020)
59
Proteome-Wide Survey of Cysteine Oxidation by Using a Norbornene Probe.
LJ Alcock, M Langini, K Stühler, M Remke, MV Perkins, GJL Bernardes, JM Chalker
Chembiochem
(2019)
21
Machine learning for target discovery in drug development
T Rodrigues, GJL Bernardes
Current Opinion in Chemical Biology
(2019)
56
A Sweet Galactose Transfer – Metabolic Oligosaccharide Engineering as a Tool to Study Glycans in Plasmodium Infection
A Kitowski, G Bernardes
(2019)
Enhancement of the Anti-Aggregation Activity of a Molecular Chaperone Using a Rationally Designed Post-Translational Modification.
PR Lindstedt, FA Aprile, MJ Matos, M Perni, JB Bertoldo, B Bernardim, Q Peter, G Jiménez-Osés, TPJ Knowles, CM Dobson, F Corzana, M Vendruscolo, GJL Bernardes
ACS Cent Sci
(2019)
5
Evaluation of linker length effects on a BET bromodomain probe.
R Traquete, E Henderson, S Picaud, PMSD Cal, F Sieglitz, T Rodrigues, R Oliveira, P Filippakopoulos, GJL Bernardes
Chemical communications (Cambridge, England)
(2019)
55
Ethynylbenziodoxolone Reactivity in Cysteine Bioconjugation
SR Adusumalli, GJL Bernardes
Chem
(2019)
5
Overexpression of osmosensitive Ca2+-activated channel TMEM63B promotes migration in HEK293T cells
M Marques, I Albuquerque, S Vaz, G Bernardes
Biochemistry
(2019)
Overexpression of Osmosensitive Ca2+-Permeable Channel TMEM63B Promotes Migration in HEK293T Cells
MC Marques, IS Albuquerque, SH Vaz, GJL Bernardes
Biochemistry
(2019)
58
Tetrazine-Triggered Release of Carboxylic-Acid-Containing Molecules for Activation of an Anti-inflammatory Drug
S Davies, L Qiao, BL Oliveira, CD Navo, G Jiménez-Osés, GJL Bernardes
ChemBioChem
(2019)
20

Group Leader

Research Interest Groups

Telephone number

01223 336305

Email address

College