News
Remarkable cytochrome P450-catalysed aromatic nitration reaction discovered by Challis group
The first example of a direct aromatic nitration reaction in natural product biosynthesis has been reported by the Challis group and collaborators at Cornell University in the leading journal Nature Chemical Biology.
When is a nanoparticle toxic?
The Gibson Group in collaboration with Pathologists from the Johannes Guttenburg University (Mainz) have published two studies onto the role of nanoparticle size and coating on their interactions with cells. The aim is to address questions regarding nanoparticle toxicity (if any). Focus was placed on cells from the vasculature (circulation). These cells are often negleted but any injected drug delivery system will encounter several kilometers of these. Several particle formations were found to enter endothelial cells associated with the blood-brain barrier - perhaps the most challenging biological barrier to drug delivery.
This work is published in Biomacromolecules: and Particle Fibre Toxicology:
(Particle Fibre Tox is No 1 Tox. Journal in ISI Citation reports, publishing Primary Research)
Establishing an independent academic career is an exciting and challenging process. The data available for UK chemistry suggests that more women than men find the process not exciting enough or too challenging. A key aspect of success in any career path is finding role models, establishing networks, and being tapped into good sources of information. Our aim is therefore to create opportunities for all of these in the first (and subsequent) Irène Joliot-Curie conference.
Unique pathway for pyrrole biosynthesis discovered
Prof. Greg Challis and Dr Lijiang Song, in collaboration with researchers at the University of Paris, report in Angewandte Chemie a hitherto unanticipated pathway for the biosynthesis of pyrroles from sugars. Using a combination of genetic engineering, isolation, structure elucidation, synthesis and feeding of biosynthetic intermediates, and incorporation of stable isotope-labelled precursors, the researchers showed that a carbohydrate, most likely N-acetylglucosamine-1-phosphate, is elaborated to the 4-acetamidopyrrole-2-carboxylate building blocks of the DNA-binding antibiotic congocidine (also known as netropsin). The assembly of pyrroles from carbohydrates is unprecedented in Nature and raises several intriguing questions regarding the mechanisms of the reactions involved. See for further details.
Nanodiamonds bring back sparkle to cleaning
Nanodiamonds have been found to help loosen crystallized fat from surfaces in a project led by Dr Andrew Marsh at University of 糖心TV. The tiny carbon particles transform the ability of surfactants to shift dirt in cold water, findings that could bring eco friendly low temperature laundry cycles.
The research is published in ACS Applied Materials and Interfaces and highlighted in the and Daily Telegraph, 26 June.
Nanodiamond Promotes Surfactant-Mediated Triglyceride Removal from a Hydrophobic Surface at or below Room Temperature Xianjin Cui, Xianping Liu, Andrew S. Tatton, Steven P. Brown, Haitao Ye, and Andrew Marsh ACS Applied Materials and Interfaces 2012,
Inhibiting Bacterial Toxins with Polymers
The Gibson group report in Angewandte Chemie: Here they probe the accessibility of carbohydrate binding sites in bacterial toxins, exemplified with the toxin produced by Vibrio cholerae, the causative agent of cholera.
Lucienne Otten and Robert Deller win Poster Prizes
Two members of the Gibson group have won poster prizes. Robert Deller won 1st Place at the RSC younger Members symposium (at Uni. Nottingham) for his work on Peptidomimetic Cryopreservation Agents. Lucienne Otten won 3rd place at the Systems Biology Annual Conference for her work on Label Free Analysis of Protein-Carbohydrate Interactions.
A new class of photoactive Pt(IV) anti-cancer prodrugs is under development in the Sadler group. But what happens when they are irradiated and how do the photoproducts interact with double-stranded DNA? Via a combination of new experimental data coupled with Ligand Field Molecular Dynamics simulations carried out in the Deeth group, we have modelled the DNA distortion caused by a putuative trans-PtII(pyridine)2 lesion. See: for all the details.
Challis group discover unprecedented alkaloid
The Challis group and collaborators at the John Innes Centre report in the journal Chemical Science on the genomics-driven discovery of a novel polyketide alkaloid with an unprecedented structure. Incorporation experiments with stable isotope-labelled precursors combined with bioinformatics analyses were used to deduce the likely biosynthetic pathway for the natural product. See for further details.
Probing Synthetic Glycan-Protein Interactions
The Gibson Group and collaborators study synthetic glycan-lectin interactions to understand the function of anti-adhesion therapies.
Smart Materials with Triggerable Membrane Interactions
The Gibson group (in collaboration with Alison Rodger) investigate how stimuli responsive polymers can be used to modulate lipophilicity.
Structural studies on a Meningitis B vaccine
Results by MOAC and chemistry PhD student Angela Martino and her supervisor Alison Rodger were published this week on 4CMenB (a new meningococcal B vaccine).