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

Cysteine-Selective Reactions for Antibody Conjugation
PMSD Cal, GJL Bernardes, PMP Gois
Angewandte Chemie International Edition
(2014)
53
A Small‐Molecule Drug Conjugate for the Treatment of Carbonic Anhydrase IX Expressing Tumors
N Krall, F Pretto, W Decurtins, GJL Bernardes, CT Supuran, D Neri
Angewandte Chemie International Edition
(2014)
53
Curative properties of noninternalizing antibody-drug conjugates based on maytansinoids.
E Perrino, M Steiner, N Krall, GJL Bernardes, F Pretto, G Casi, D Neri
Cancer Res
(2014)
74
Rationally designed short polyisoprenol-linked PglB substrates for engineered polypeptide and protein N-glycosylation
F Liu, B Vijayakrishnan, A Faridmoayer, TA Taylor, TB Parsons, GJL Bernardes, M Kowarik, BG Davis
Journal of the American Chemical Society
(2014)
136
Rationally Designed Short Polyisoprenol-Linked PglB Substrates for Engineered Polypeptide and Protein N-Glycosylation
F Liu, B Vijayakrishnan, A Faridmoayer, TA Taylor, TB Parsons, GJL Bernardes, M Kowarik, BG Davis
J Am Chem Soc
(2013)
136
Protein micro- and nano-capsules for biomedical applications
U Shimanovich, GJL Bernardes, TPJ Knowles, A Cavaco-Paulo
Chem Soc Rev
(2013)
43
Highlights from the 48th EUCHEM conference on stereochemistry, Bürgenstock, Switzerland, May 2013.
GJL Bernardes
Chemical communications (Cambridge, England)
(2013)
49
Site-specific chemical modification of antibody fragments using traceless cleavable linkers.
GJL Bernardes, M Steiner, I Hartmann, D Neri, G Casi
Nature Protocols
(2013)
8
Synthetically defined glycoprotein vaccines: Current status and future directions
R Adamo, A Nilo, B Castagner, O Boutureira, F Berti, GJL Bernardes
Chem Sci
(2013)
4
Chemoselective transformations for bioimaging and targeted therapeutics
GJL Bernardes
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS
(2013)
42

Group Leader

Research Interest Groups

Telephone number

01223 336305

Email address

College