skip to content

Yusuf Hamied Department of Chemistry

 

Professor of Chemical and Molecular Biology

Protein Folding and Assembly

Our research focuses on different aspects of how proteins fold and how large protein complexes assemble. Projects cover diverse areas including biophysics, molecular biology (including protein engineering) and chemical biology. Current projects include:

How does a knotted protein fold?

Recently, a remarkable new class of proteins have been discovered which have deep topological knots formed by the polypeptide backbone. These structures represent a new challenge for the protein folding community - not only has the protein to fold but in doing so it must also knot. We are studying the folding pathways of several knotted proteins, including YibK shown on the right, using a combination of experimental and computational techniques.

How do molecular chaperones work to assembly large molecular complexes?

Heat shock protein 90 (Hsp90) is a highly abundant and important protein in our cells which is the target of a new class of anti-tumour agents. It plays a key role in the assembly of a number of cellular complexes which are critical in cellular signal transduction pathways. We are combining a large number of biophysical techniques to understand the mode of action of Hsp90.

Single molecule studies on the folding of a large β-barrel protein.

The green fluorescent protein (GFP) first isolated from jellyfish is a protein with unique spectroscopic properties. A cyclisation and oxidation of the polypeptide backbone results in the formation of a chromophore which is highly fluorescent. In collaboration with the Klenerman group are using these special features of GFP to study the folding of this protein at a single molecule level.

Selected Publications

  • Mallam, A.L., Rogers, J.M. and Jackson, S.E. (2010) Proc. Natl. Acad. Sci. 107, 8189-8194. Experimental detection of knotted conformations in denatured proteins
  • Hsu, D., Blaser, G., Behrens, C., Cabrita, LD., Dobson, C.M. and Jackson, S.E. (2010) J. Biol. Chem. 285, 4859-4869. Folding Study of Venus Reveals a Strong Ion Dependence of its Yellow Fluorescence under Mildly Acidic Conditions
  • Onuoha, S.C., Coulstock, E.C., Grossmann, J.G. and Jackson, S.E. (2008) J. Mol. Biol. 379, 732-744. Structural studies on the co-chaperone Hop and its complexes with Hsp90
  • Mallam, A.L., Onuoha, S.C., Grossmann, J.G. and Jackson, S.E. (2008) Molecular Cell 30, 642-648. Knotted fusion proteins reveal unexpected possibilities in protein folding
  • Orte, A., Craggs, T.D., White, S. Jackson, S.E. and Klenerman, D. (2008) J. Am.Chem.Soc. 130, 7898-7907. Evidence of an intermediate and parallel pathways in protein unfolding using single-molecule fluorescence

Watch Professor Jackson discuss her research

Take a tour of the Jackson Lab

Publications

Folding study of Venus reveals a strong ion dependence of its yellow fluorescence under mildly acidic conditions.
S-TD Hsu, G Blaser, C Behrens, LD Cabrita, CM Dobson, SE Jackson
– Journal of Biological Chemistry
(2010)
285,
4859
Backbone assignments of the 26 kDa neuron-specific ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1)
FI Andersson, SE Jackson, S-TD Hsu
– Biomolecular NMR Assignments
(2009)
4,
41
The folding, stability and conformational dynamics of beta-barrel fluorescent proteins
S-TD Hsu, G Blaser, SE Jackson
– Chemical Society Reviews
(2009)
38,
2951
The discovery and development of the green fluorescent protein, GFP.
JKM Sanders, SE Jackson
– Chemical Society Reviews
(2009)
38,
2821
Untangling the folding mechanism of the 52‐knotted protein UCH‐L3
FI Andersson, DG Pina, AL Mallam, G Blaser, SE Jackson
– The FEBS Journal
(2009)
276,
2625
Single Molecule Studies Of Ubiquitin Unfolding
S Ibrahim, G Blaser, A Orte, S Jackson, D Klenerman
– Biophysical Journal
(2009)
96,
555A
Folding and stability of the ligand-binding domain of the glucocorticoid receptor
SH McLaughlin, SE Jackson
– Protein science : a publication of the Protein Society
(2009)
11,
1926
Exploring knotting mechanisms in protein folding
AL Mallam, ER Morris, SE Jackson
– Proceedings of the National Academy of Sciences of the United States of America
(2008)
105,
18740
The extremely slow-exchanging core and acid-denatured state of green fluorescent protein
J-R Huang, S-TD Hsu, J Christodoulou, SE Jackson
– HFSP journal
(2008)
2,
378
Knotted Fusion Proteins Reveal Unexpected Possibilities in Protein Folding
AL Mallam, SC Onuoha, JG Grossmann, SE Jackson
– Mol Cell
(2008)
30,
642
  • <
  • 7 of 13
  • >

Research Group

Research Interest Group

Telephone number

01223 336357 (shared)
01223 762011

Email address

sej13@cam.ac.uk

College

Peterhouse