Christopher Hamilton


  • 2.33A Chemistry

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Personal profile


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Chris Hamilton graduated from the University of Liverpool (1994) and got his PhD (1997) from the University of Exeter working with Prof. Stan Roberts on the synthesis of biologically stable nor-carbovir triphosphate analogues as inhibitors of HIV reverse transcriptase. This was followed by postdoctoral appointments with Prof David Gani working on ‘protein phosphatase assay development’ (St Andrews, 1998) and Dr Ian Eggleston/Prof Alan Fairlamb ‘synthesis of lunaria alkaloids & mechanistic studies as trypanothione reductase inhibitors’, (Dundee, 1999-2000). He then worked at UEA with Prof. Rob Field, first as a postdoctoral researcher (Studying Bordetella pertussis lipopolysaccharide biosynthesis, 2001) and then as a fixed term lecturer (2002). Shortly after receiving a Wellcome Trust SHOWCASE award, he took up post as Lecturer in Organic Chemistry at Queen’s University Belfast in late-2003. He returned to UEA (late 2007). His research interests reside at the Chemistry/Biology interface. This is exemplified by the cross section of research group members, which includes researchers with expertise in synthetic chemistry, biochemistry, microbiology and plant biology. Current research interests are focussed in the following areas:-

  • Chemical and biochemical functions of low molecular weight thiols in Gram positive bacteria.
  • Redox mechanisms of bioactive organosulfur metabolites from garlic
  • Mechanistic enzymology

Dr Hamilton is part of the Medicinal Chemistry Group.

Selected publications

Mechanistic studies of FosB: a divalent metal-dependent bacillithiol-S-transferase that mediates fosfomycin resistance in Staphylococcus aureus
A.A. Roberts, S.V. Sharma, A.W. Strankman, S.R. Duran, M. Rawat, C.J. Hamilton*
Biochem. J. 2013, 451, 69-79
DOI: 10.1042/BJ20121541

Distribution and infection related functions of bacillithiol in Staphylococcus aureus
D. Pöther, P. Gierok, M. Harms3, J. Mostertz, F. Hochgräfe, H. Antelmann, C.J. Hamilton, I. Borovok, M. Lalk, Y. Aharonowitz, M. Hecker*
Int. J. Med. Microbiol. 2012 (in press)
DOI: 10.1016/j.ijmm.2013.01.003

Chemical and chemoenzymatic syntheses of bacillithiol: A unique low molecular-weight thiol amongst low G + C Gram-positive bacteria.
Sunil V. Sharma, Vishnu K. Jothivasan, Gerald L. Newton, Heather Upton, Judy I. Wakabayashi, Melissa G. Kane, Alexandra A. Roberts, Mamta Rawat, James J. La Clair, Chris J. Hamilton
Angewandte Chemie International Edition, 2011, 50, 31, 7101–7104
DOI: 10.1002/anie.201100196

Bacillithiol is an antioxidant thiol produced in Bacilli.
G. L. Newton, M. Rawat, J. J. La Clair, V. K. Jothivasan, T. Budiarto, C. J. Hamilton, Al Claiborne, J. D. Helmann, R. C. Fahey*,
Nat. Chem. Biol. 2009, 625-627.

Mycothiol disulfide reductase:- A continuous assay for slow time-dependent inhibitors.
C. J. Hamilton,* R. M. J. Finlay, M. J.G. Stewart, A. Bonner.
Analytical Biochem., 2009, 388, 91-96.

Nucloside triphosphate mimicry:- A sugar triazolyl nucleoside as an ATP-competitive inhibitor of B. anthracis pantothenate kinase.
A.S. Rowan, N.I. Nicely, N. Cochrane, W.A. Wlassoff, A. Claiborne, C.J. Hamilton.
Org. Biomol. Chem. 2009, 7, 4029-4037.
DOI: 10.1039/b909729e

Key Research Interests

Our research programs embrace a diverse range of disciplines such as Synthetic Chemistry, Biotransformations, Enzymology, Biochemistry and Molecular/Microbiology. This facilitates the design, synthesis and application of novel chemical tools to address complex biological/medicinal challenges. Traversing these disciplinary boundaries provides a stimulating interdisciplinary research culture, and excellent research training/experience, across the full spectrum of the chemical/life sciences interface from the extremes of Synthetic Organic Chemistry to Cell Biology and beyond.

Bacillithiol: A unique low molecular weight thiol cofactor amongst many low G+C Gram positive bacteria
Glutathione (GSH) is the major low molecular weight (LMW) thiol in eukaryotes and many gram negative bacteria. GSH plays a critical role in disulfide stress management and maintaining an intracellular reducing environment via the chemical and/or enzymatic reduction of toxic oxidants. Protein glutathionylation (reversible formation of GS-S-protein disulfides) is also an important post-translational modification for regulating protein function and protecting exposed cysteine (Cys) residues from irreversible damage during oxidative stress.[1] Glutathione-S-transferases mediate xenobiotic metabolism/detoxification via S-conjugation with GSH. Gram positive bacteria lack GSH, but instead produce other LMW thiols (eg. mycothiol in Actinomycetes), which have functions analogous to GSH.[2] Recently, as part of an international and interdisciplinary research collaboration we helped characterise Bacillithiol (BSH) as the major, cysteine-containing, low molecular weight thiol amongst many low G+C Gram positive bacteria, which do not produce MSH or GSH.[3] These include Bacillus anthracis (anthrax), B. cereus (food poisoning), Staphylococcus aureus (bacterial sepsis), B. subtilis (soil bacterium and genetic model for the Bacilli) and Deinococcus radiodurans (a polyextremophile and the world’s toughest bacterium). The major focus of our recent[4][5] and ongoing research efforts is to elucidate the fundamental aspects of BSH biosynthesis and its roles in redox regulation, xenobiotic detoxification and metal ion homeostasis. Many of these projects also involve extensive collaborations with research groups with complementary expertise in microbiology, structural biology and proteomics. We have recently completed total syntheses of BSH, its symmetrical disulfide (BSSB) and all of its biosynthetic precursors.[4] Synthetic BSH has already been used to establish that the fosfomycin resistance protein (FosB)[5] found in low G+C gram positive bacteria is a bacillithiol-S-transferase for which bacillithiol is a preferred thiol substrate compared to cysteine or GSH.[4]

References: [1] Free Rad. Biol. Med. 2007, 43, 883; [2] Nat. Prod. Rep. 2008, 25, 1091; [3] Nat. Chem. Biol. 2009, 625-627; [4] Biochemistry, 2010, 49, 8398-8414; [4] Angew. Chemie Int. Ed. 2011, 50, 7101-7104. [5] J. Bacteriol. 2001, 183, 2380-2383. BSH is now commercially available from JEMA Biosciences

Garlic-derived diallyl-polysulfides: Mechanistic studies and their application as antifungal, antimicrobial and nematocidal agents
There is considerable interest in the development of new pesticides based on organosulfur metabolites from garlic, since such food-based products are environmentally benign. Garlic (Allium sativum) contains a wide range of such organosulfur metabolites with distinct biological activities. When garlic is crushed, the enzyme alliinase converts alliin into allicin, a highly reactive thiosulfoxide. Several bioactive degradation products are subsequently formed such as diallyl polysulfides (DAPS). Little is known about the mode(s) of action of these compounds. We are investigating how their bioactivity can be triggered and/or neutralised by low molecular weight thiols within prokaryotic/eukaryotic cells, how this impacts on the intracellular redox status and how this relates to their observed nematicidal, antifungal and antibacterial activities. A more detailed knowledge of the intracellular redox reactions induced by different DAPS will help to distinguish between the mode of action of different DAPS and can result in an improved use of the compounds in agriculture and medicine.

This project is supported and being pursued in close collaboration with ECOspray Ltd. ( who have developed and registered several, environmentally benign, agricultural/horticultural/amenity pesticides formulated from garlic extracts.

References: [1] Org. Biomol. Chem. 2007, 1505. [2] E. Bloc. Garlic and other alliums, The lore and the science, Royal Society of Chemistry, Cambridge, ISBN: 978-85404-190-9.

Mycothiol Disulfide Reductase (Mtr)
Mycothiol (MSH) is the major small molecule thiol found in M. tuberculosis which plays a key role in oxidative stress management.[1] The NADPH-dependent oxidoreductase mycothiol disulfide reductase (mtr) is responsible for recycling the disulfide (MSSM) back to MSH and thereby maintaining an intracellular reducing environment.[2] Further studies into the biological significance of the mycothiol redox cycle are currently hampered by the limited availability of mycothiol. We have recently developed an efficient synthesis of simplified mycothiol disulfide analogues that can be used as alternative substrate substrates for mtr[3] that are suitable for substrate-economic mycothiol disulfide reductase assays.[4] These assays are now being used to investigate the biological mechanisms of anti-tubercular natural products isolated from native flora in South Africa and Tanzania. References: [1] Nat. Prod. Rep. 2008, 25, 1091-1117; [2] Biochemistry, 2001, 40, 5119-5126; [3] Org. Biomol. Chem. 2008, 6, 385-390; [4] Analytical Biochem. 2009, 388, 91-96
Kinetic/Inhibition studies of B. anthracis pantothenate kinase

CoenzymeA (CoASH) is an essential biological cofactor (eg. as the major acyl-group carrier) whose biosynthetic pathway is also highly conserved across all organisms. The first obligate step in CoASH biosynthesis is the phosphorylation of pantothenate (Pan) by pantothenate kinase (PanK). To date, three bacterial PanK isoforms (PanKs-I-III) have been classified based on primary sequence and substrate/inhibitor specificities. Sequence similarity amongst PanKs I–III is N-5-pantothenamide 1 as an alternative substrate, but only type-I PanKs are susceptible to feedback inhibition by CoASH.1 The type-III enzymes cannot phosphorylate 1, nor are they inhibited by CoASH.2 The pantothenate binding pocket of type I-II PanKs includes a hydrophobic cavity that enables them to accommodate the extended alkyl chain of 1 and to use it as an alternative substrate. Type-III PanKs lack this hydrophobic pocket hence they cannot bind and phosphorylate 1. Structures of type-II S. aureus kinase (saPanK)3 and type-III kinase utilised by Bacillus anthracis kinase (baPanK)4have been determined and pantothenate mimetics 1-5 have also been reported as inhibitors/substrates of saPanK.5    

We are specifically interested in the B. anthracis type-III panK enzyme and are currently studying the substrate/inhibitor properties of known pantothenate mimetics (1-5) and novel analogues (prepared in-house). In Collaboration with Prof. Al Claiborne (Wake Forest University, N. Carolina) and Asinex (Moscow)  

References [1] Strauss et al, J. Biol. Chem. 2002, 277, 48205; [2] Brand et al, J. Biol. Chem. 2005, 280, 20185; [3] Hong et al, Structure, 2006, 14, 1251; [4] Nicely et al Biochemistry, 2007, 46, 3234. [5] Virga et al, Bioorg. Med. Chem., 2006, 14, 1007

Research Funding

Research Enterprise & Engagement UEA Proof of concept fund
Scale-up preparation and distribution of Bacillithiol
C. Hamilton
May-11 to Jul-11
Marie Curie ITN & ECOspray Ltd

Antifungal, antimicrobial and nematocidal studies of garlic-derived diallyl-polysulfides
C. Hamilton
Oct-10 to Sep-13

Research Enterprise & Engagement UEA Proof of concept fund
Synthesis of expensive fine chemicals with therapeutic potential.
C. Hamilton, C. Brearley
Aug-10 to Jul-11

Nuffield Foundation undergraduate research bursary
Synthesis and Evaluation of Competitive Inhibitors of Pantothenate Kinase.
T. Powell-Davis, C. Hamilton
Jul-10 to Aug-10

Wellcome Trust vacation scholarship
Kinetic inhibition studies of BshA, the glycosyltransferase, which catalyses the first biosynthetic step of the unique thiol cofactor, bacillithiol, amongst pathogenic Bacilli
C. Mitrofan, C. Hamilton
Jun-10 to Jul-10

BBSRC Responsive Mode
Bacillithiol and its unique drug resistance pathways in Bacilli
C. Hamilton
Apr-10 to Sep-12

Nuffied Foundation
Synthesis & evaluation of a selective colorimetric disulfide titrant
C.J. Hamilton
Jul 2007 – Aug 2007
£ 1360

Wellcome Trust
Substrate/inhibition kinetics of pantothenate analogues against Bacillus Anthracis pantothenate kinase
C.J. Hamilton
Jul 2007 - Aug-2007

Royal Society
Unveiling the mycothiol proteome
M. Rawat, C.J. Hamilton
Jul 2007 - Aug 2007
£ 2496

A chemoselective ligation approach to glycosyltransferase bisubstrate mimetics
C.J. Hamilton
Jul 2007 - Jun 2009
£ 228,532

Marie Curie Host Fellowships
New methods to synthesise unnatural nucleosides, known and putative antiproliferative agents
M. Migaud, C.J. Hamilton, D. Boyd, J. Mann
€ 626,507

Wellcome Trust
CMP-Neu5Ac synthetase catalysed synthesis of sugar-NMPs
C.J. Hamilton
Jul 2005 – Aug 2005
£ 1320

Royal Society / NRF
Scientific validation of South African plants for anti-TB, anti-diabetes and anti-tyrosinase activity
N. Lall, J.J. Marion, P. Houghton, C.J. Hamilton
R 175000

Wellcome Trust
13C-labelled acrylonitriles for mechanistic studies of covalent inhibitors of disulfide reductases
C.J. Hamilton
Jul 2004 – Aug 2004
£ 1,280

Nuffield Foundation
Synthetic/mechanistic studies of 13C-labelled time-dependent inhibitors of trypanothione reductase
C.J. Hamilton
Jul 2003 –Aug 2003
£ 1,596

Wellcome Trust
Cell Permeable NTP Analogues as Tools for Chemotherapy, Cell Biology and Chemical Genetics
C.J. Hamilton
Apr 2003 – Sep 2005
£ 125,000

Wellcome Trust
A Substrate-Economic High-Throughput Inhibition Assay for Mycothione Reductase
C.J. Hamilton
Jul 2002 – Aug 2002
£ 1160

Guildford Bench Methodology Fund
A Substrate-Economic High-Throughput Inhibition Assay for Mycothione Reductase
C.J. Hamilton
Jul 2002 – Aug
£ 920

Research Group or Lab Membership

Miriam Arbach (Plant Biologist/Biochemist)
Dr Alexandra Roberts (Microbiologist/Biochemist)
Dr Sunils Sharma (Synthetic Chemist)

Expertise related to UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  • SDG 3 - Good Health and Well-being
  • SDG 11 - Sustainable Cities and Communities

Collaborations and top research areas from the last five years

Recent external collaboration on country/territory level. Dive into details by clicking on the dots or