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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

Evidence of an Intermediate and Parallel Pathways in Protein Unfolding from Single-Molecule Fluorescence
A Orte, TD Craggs, SS White, SE Jackson, D Klenerman
– Journal of the American Chemical Society
(2008)
130,
7898
The Solution to Multiple Structures
SE Jackson
– Structure (London, England : 1993)
(2008)
16,
659
Structural studies on the co-chaperone hop and its complexes with Hsp90
SC Onuoha, ET Coulstock, JG Grossmann, SE Jackson
– Journal of Molecular Biology
(2008)
379,
732
Use of Protein Engineering Techniques to Elucidate Protein Folding Pathways
AL Mallam, SE Jackson
– Progress in molecular biology and translational science
(2008)
84,
57
Spin relaxation effects in photochemically induced dynamic nuclear polarization spectroscopy of nuclei with strongly anisotropic hyperfine couplings.
I Kuprov, TD Craggs, SE Jackson, PJ Hore
– J Am Chem Soc
(2007)
129,
9004
Mechanistic studies on Hsp90 inhibition by ansamycin derivatives.
SC Onuoha, SR Mukund, ET Coulstock, B Sengerovà, J Shaw, SH McLaughlin, SE Jackson
– Journal of molecular biology
(2007)
372,
287
Conformational dynamics of the molecular chaperone Hsp90 in complexes with a co-chaperone and anticancer drugs
JJ Phillips, ZP Yao, W Zhang, S McLaughlin, ED Laue, CV Robinson, SE Jackson
– J Mol Biol
(2007)
372,
1189
Stable intermediate states and high energy barriers in the unfolding of GFP
J-R Huang, TD Craggs, J Christodoulou, SE Jackson
– Journal of molecular biology
(2007)
370,
356
Destabilised mutants of ubiquitin gain equal stability in crowded solutions.
A Roberts, SE Jackson
– Biophys Chem
(2007)
128,
140
YFP unfolding kinetics studied in a single-molecule nano-flow cell
A Orte, TD Craggs, SS White, SE Jackson, D Klenerman
– BIOPHYSICAL JOURNAL
(2007)
660A
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Research Group

Research Interest Group

Telephone number

01223 336357 (shared)
01223 762011

Email address

sej13@cam.ac.uk

College

Peterhouse