Researchers have created a new synthetic class of helix-shaped molecules which they believe could be a key tool in the worldwide battle against antibiotic resistance. By twisting molecules around iron atoms they have created what they term ‘flexicates’ which are active against MRSA and E-coli - but which also appear to have low toxicity , reducing the potential for side effects if used in treatment. The work is published in Nature Chemistry.
The new structures harness the phenomenon of ‘chirality’ or ‘handedness’ whereby the corkscrew molecules could be left-handed or right-handed. By making the most effective ‘hand’ to attack a specific disease, the University of Warwick research paves the way towards a more targeted approach to killing pathogens. In the case of E-coli and MRSA, it is the left ‘hand’ which is most effective.
Professor Peter Scott of the University of Warwick’s chemistry department said although this particular study concentrated on flexicates’ activity against MRSA and E-coli, the new method of assembly could also result in new treatments for other diseases.
“It’s a whole new area of chemistry that really opens up the landscape to other practical uses. These new molecules are synthetically flexible, which means that with a bit of tweaking they can be put to use against a whole host of different diseases, not just bugs like MRSA which are rapidly developing resistance to traditional antibiotics. Flexicates are also easier to make and produce less waste than many current antibiotics.”
Scientists have long been able to copy nature’s corkscrew-shaped molecules in man-made structures known as helicates – but they have thus far not been able to use them in fighting diseases. One of the key issues is the problem of handedness. Sometimes ‘left-handed’ molecules in drugs are the most effective at combating some disease, while sometimes the ‘right-handed’ version works best. Until now, scientists working with helicates have found it difficult to make samples containing just one type of corkscrew; either the right- or left-handed twist.
With flexicates, the University of Warwick scientists have succeeded in making samples containing just one type of twist – resulting in a more targeted approach which would allow the drug dosage to be halved. Flexicates solve other problems encountered by helicates, as they are easier to optimise for specific purposes, are better absorbed by the body and are easier to mass-produce synthetically.
Professor Scott said: “Drugs often have this property of handedness - their molecules can exist in both right and left handed versions but the body prefers to use only one of them. For this reason, drug companies have to go to the trouble of making many traditional molecules as one hand only. What we have done is solve the ‘handedness’ problem for this new type of drug molecule. By getting the correct hand we can halve the drug dose, which has the benefits of minimising side effects and reducing waste. For patients, it’s safer to swallow half the amount of a drug. Our work means that we can now make whichever hand of the corkscrew we want, depending on the job we require it to do.”
Notes to editors
The study, entitled Optically pure, water-stable metallo-helical ‘flexicate’ assemblies with antibiotic activity, is published in Nature Chemistry.
The research was also supported financially by EPSRC.
It is authored by Peter Scott, Suzanne Howson, Guy Clarkson and Alison Rodger from the University of Warwick, Albert Bolhuis from the University of Bath and Viktor Brabec and Jaroslav Malina from the Academy of Sciences of the Czech Republic.
When the paper is published it can be retrieved at http://dx.doi.org/10.1038/NCHEM.1206
Professor Peter Scott is available on +44 (0) 24 7652 3238 or firstname.lastname@example.org
University of Warwick press officer Anna Blackaby is available on + 44 (0) 2476 575910 or + 44 (0)7785 433155 or email@example.com