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

Direct radiolabelling of proteins at cysteine using [18F]- fluorosugars
O Boutureira, GJL Bernardes, F D'Hooge, BG Davis
Chemical Communications
(2011)
47
Methods for converting cysteine to dehydroalanine on peptides and proteins
JM Chalker, SB Gunnoo, O Boutureira, SC Gerstberger, M Fernández-González, GJL Bernardes, L Griffin, H Hailu, CJ Schofield, BG Davis
Chemical Science
(2011)
2
Towards improved therapeutic CORMs: understanding the reactivity of CORM-3 with proteins.
T Santos-Silva, A Mukhopadhyay, JD Seixas, GJL Bernardes, CC Romão, MJ Romão
Curr Med Chem
(2011)
18
Site‐Selective Traceless Staudinger Ligation for Glycoprotein Synthesis Reveals Scope and Limitations
GJL Bernardes, L Linderoth, KJ Doores, O Boutureira, BG Davis
Chembiochem : a European journal of chemical biology
(2011)
12
A "tag-and-modify" approach to site-selective protein modification
JM Chalker, GJL Bernardes, BG Davis
Accounts of Chemical Research
(2011)
44
A Coordinated Synthesis and Conjugation Strategy for the Preparation of Homogeneous Glycoconjugate Vaccine Candidates
EJ Grayson, GJL Bernardes, JM Chalker, O Boutureira, JR Koeppe, BG Davis
Angewandte Chemie International Edition
(2011)
50
CORM-3 Reactivity toward Proteins: The Crystal Structure of a Ru(II) Dicarbonyl-Lysozyme Complex
T Santos-Silva, A Mukhopadhyay, JD Seixas, GJL Bernardes, CC Romão, MJ Romão
Journal of the American Chemical Society
(2011)
133
Chemical Site-selective Modification of Proteins: Tools for Synthetic Biology
GJL Bernardes
FASEB JOURNAL
(2011)
25
Site-selective chemoenzymatic construction of synthetic glycoproteins using endoglycosidases
M Fernández-González, O Boutureira, GJL Bernardes, JM Chalker, MA Young, JC Errey, BG Davis
Chemical Science
(2010)
1
Design, synthesis and biological evaluation of carbohydrate-functionalized cyclodextrins and liposomes for hepatocyte-specific targeting.
GJL Bernardes, R Kikkeri, M Maglinao, P Laurino, M Collot, SY Hong, B Lepenies, PH Seeberger
Org Biomol Chem
(2010)
8

Group Leader

Research Interest Groups

Telephone number

01223 336305

Email address

College