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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

The dimerization of an α/β-knotted protein is essential for structure and function
AL Mallam, SE Jackson
– Structure
(2007)
15,
111
A comparison of the folding of two knotted proteins: YbeA and YibK.
AL Mallam, SE Jackson
– J Mol Biol
(2006)
366,
650
Ubiquitin: A Small Protein Folding Paradigm
SE Jackson
– ChemInform
(2006)
37,
no
19F NMR studies of the native and denatured states of green fluorescent protein.
F Khan, I Kuprov, TD Craggs, PJ Hore, SE Jackson
– Journal of the American Chemical Society
(2006)
128,
10729
Probing nature's knots: the folding pathway of a knotted homodimeric protein.
AL Mallam, SE Jackson
– J Mol Biol
(2006)
359,
1420
Ubiquitin: a small protein folding paradigm.
SE Jackson
– Organic & biomolecular chemistry
(2006)
4,
1845
The co-chaperone p23 arrests the Hsp90 ATPase cycle to trap client proteins.
SH McLaughlin, F Sobott, ZP Yaol, W Zhang, PR Nielsen, JG Grossmann, ED Laue, CV Robinson, SE Jackson
– J Mol Biol
(2005)
356,
746
The latest in Engineering and design: The 2005 collection
SE Jackson, L Regan
– Current Opinion in Structural Biology
(2005)
15,
432
A recurring theme in protein engineering: the design, stability and folding of repeat proteins.
ERG Main, AR Lowe, SGJ Mochrie, SE Jackson, L Regan
– Current opinion in structural biology
(2005)
15,
464
Ubiquitin folds through a highly polarized transition state.
HM Went, SE Jackson
– Protein engineering, design & selection : PEDS
(2005)
18,
229
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Research Group

Research Interest Group

Telephone number

01223 336357 (shared)
01223 762011

Email address

sej13@cam.ac.uk

College

Peterhouse