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New technology to revolutionise drug development

5th June 2019


The search for new drugs to combat diseases more effectively could be revolutionised through a new £30 million electron microscopy project.

Experts would be able to see, for the first time, how a particular drug works within a patient at a cellular level or the molecular processes set in motion by a genetic mutation.

The technology aims to create 3D images of cells at very high resolution to transform our understanding of diseases such as cancer and revolutionise how new medicines are designed.

The project based at Harwell, in Oxfordshire, will be supported with £3 million from the government's Office for Life Sciences and led by Thermo Fisher Scientific and the Rosalind Franklin Institute, which is dedicated to bringing about transformative changes through research and technology development. 

Professor James Naismith, lead researcher and Director of the Rosalind Franklin Institute, said: "Around 80% of new drugs fail when they reach clinical trials because we don¹t fully understand their effects within a living organism. We're currently able to identify genes and proteins that play a role in diseases but can only study these in detail in isolation, not as part of a whole cell or group of cells. This new technology would be the first to allow us to do that, so we can see the full effects of a drug and identify at a much earlier stage what will work and what will not.

"Drug development has never been slower or higher cost than it is now. We need to have a breakthrough in the physical science that supports drug discovery to change that."

The project was announced as work begins on the Rosalind Franklin Institute's central hub building on the Harwell Campus near Oxford. The building will create a specialist environment for sensitive scientific equipment that will be unique in the world. It is set to house 200 researchers and will open in late 2020.

The new imaging technique will be based on a technology called cryogenic electron tomography (cryo-ET), which builds up a 3D image from multiple 2D images of samples which have been flash frozen at temperatures below -180oC. 

Although cryo-ET already exists, it can currently only handle small samples, such as parts of cells, and often requires in-house expertise.

Mike Shafer, president of materials and structural analysis at Thermo Fisher Scientific said: "Our company¹s mission is to enable our customers to make the world healthier, cleaner and safer, and our collaboration with the Rosalind Franklin Institute, Diamond Light Source and others to develop a more efficient cryo-tomography solution, maps precisely to that vision. Our combined goal is to make this technique widespread so scientists and researchers in academic institutions and the biopharmaceutical industry can better understand disease mechanisms at the cellular level, leading to faster drug discovery and cures for neurodegenerative diseases, cancers and other debilitating illnesses."

The new, five-year research project will rapidly speed up the technique to process much larger samples including patient biopsies, increase workflow automation and standardise post-processing data. The long-term aim is to bring the technology closer to the clinic so it can be used in both research hospitals and laboratories.

The challenges around the project are formidable. It will require the invention of new techniques for preparing and handling samples of human tissue that are less than a hundredth of the thickness of human hair.

It will involve the design of new electron microscopy techniques to speed up the imaging process and collect the huge amount of data created. New software and machine learning technology will need to be developed to process this data in order to create and interpret the 3D images.





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