One of the biggest challenges in biological chemistry is the design of small molecules that interact selectively with macromolecules. We are pioneering the development of the use of fragments to address this challenge. This approach involves close synergistic interaction between synthetic organic chemistry, biophysics and structural biology. We are using fragment-based methods to identify inhibitors of enzymes from Mycobacterium tuberculosis, and to develop small molecules that modulate protein-protein interactions. We are also keen to explore new applications for fragments e.g. to identify molecules that modulate the activity of riboswitches, and to assign function to orphan proteins.

Our second major area of research is to develop the use of microdroplets in microfluidics as a novel experimental platform for biological chemistry. This research is highly interdisciplinary and involves biological chemistry, microfluidics, nanofabrication, laser spectroscopy and mass spectrometry. We are particularly interested in looking at cells in droplets, e.g. bacteria to study quorum sensing, algae for bio-fuel development.
AFFINITY LABELING OF ESCHERICHIA-COLI DEHYDROQUINASE
TDH BUGG, C ABELL, JR COGGINS - TETRAHEDRON LETT (
1988)
29, 6783
(DOI:
10.1016/S0040-4039(00)82454-5)
STUDIES ON THE BIOSYNTHESIS OF HYDROXYMELLEIN USING O-17 NMR AND H-2 NMR-SPECTROSCOPY TO DETERMINE THE ORIGIN OF THE C-4 HYDROXY GROUP
C ABELL, AC SUTKOWSKI, J STAUNTON - Journal of the Chemical Society, Chemical Communications (
1987), 586
(DOI:
10.1039/c39870000586)
EVIDENCE FOR CONSECUTIVE 1,2-ALKYL SHIFTS IN STERPURENE BIOSYNTHESIS - ISOLATION AND CHARACTERIZATION OF 7,12-DIHYDROXYSTERPURENE
C ABELL, AP LEECH - Tetrahedron Letters (
1987)
28, 4887
(DOI:
10.1016/S0040-4039(00)96652-8)
Purification, N-terminal amino acid sequence and properties of hydroxymethylbilane synthase (porphobilinogen deaminase) from Escherichia coli
GJ HART, C ABELL, AR BATTERSBY - Biochemical Journal (1986) 240, 273
The use of nmr spectroscopy to follow deuterium in studies of fungal metabolism
C Abell - (1986) 2
BIOMIMETIC SYNTHESES OF THE POLYKETIDE FUNGAL METABOLITES ALTERNARIOL AND RUBROFUSARIN - MODELS FOR CYCLIZATION REACTIONS CATALYZED BY POLYKETIDE SYNTHASE ENZYMES
C ABELL, BD BUSH, J STAUNTON - Journal of the Chemical Society, Chemical Communications (
1986), 15
(DOI:
10.1039/c39860000015)
BIOSYNTHESIS OF 6-METHYLSALICYLIC ACID - THE COMBINED USE OF MONO-DEUTERIATED AND TRI-DEUTERIATED ACETATE PRECURSORS TO INVESTIGATE THE DEGREE OF STEREOCONTROL IN THE AROMATIZATION SEQUENCE
C ABELL, J STAUNTON - Journal of the Chemical Society, Chemical Communications (
1984), 1005
(DOI:
10.1039/c39840001005)
BIOSYNTHESIS OF THE POLYKETIDE MELLEIN FROM CD3CO2H AND (CD3CO2H)-C-13 IN ASPERGILLUS-MELLEUS - DETECTION OF DEUTERIUM BY H-2 NMR AND EDITED C-13 NMR-SPECTRA
C ABELL, DM DODDRELL, MJ GARSON, ED LAUE, J STAUNTON - Journal of the Chemical Society, Chemical Communications (
1983), 694
(DOI:
10.1039/c39830000694)
BIOSYNTHESIS OF THE FUNGAL METABOLITES ALTERNARIOL, MELLEIN, RUBROFUSARIN, AND 6-METHYLSALICYLIC ACID FROM CD3CO2H
C ABELL, MJ GARSON, FJ LEEPER, J STAUNTON - Journal of the Chemical Society - Series Chemical Communications (
1982)
No. 17, 1011
(DOI:
10.1039/c39820001011)
THE USE OF H-2 NMR-SPECTROSCOPY AND BETA-ISOTOPIC SHIFTS IN THE C-13 NMR-SPECTRUM TO MEASURE DEUTERIUM RETENTION IN THE BIOSYNTHESIS OF THE POLYKETIDE 6-METHYLSALICYLIC ACID
C ABELL, J STAUNTON - Journal of the Chemical Society, Chemical Communications (
1981), 856
(DOI:
10.1039/c39810000856)