Breakthrough hope for host of new medicines

A METHOD of re-shaping complex biological molecules by “directing” evolution could lead to a host of new medicines, according to a US study.

The technique uses a virus that infects bacteria to accelerate the mutation rate of genes for therapeutic proteins.

Phage-assisted continuous evolution (Pace) is said to be 100 times faster than conventional ways of producing large “macromolecules” such as enzymes that can fight disease.

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Research leader Professor David Liu, from Harvard University, said: “Most modern drugs are based on small organic molecules, but biological macromolecules may be better suited as pharmaceuticals in some cases. Our work provides a new solution to one of the key challenges in the use of macromolecules as research tools or human therapeutics: how to rapidly generate proteins or nucleic acids with desired properties.”

The scientists used “phage” viruses to transfer evolving genes between a series of E.coli bacteria.

At each step, the genes produce within the bacteria an altered version of the proteins they code for.

The virus has a life cycle of just 10 minutes. As a result, the researchers were able to achieve 60 rounds of protein evolution every 24 hours. The process would normally take years.