Laser Tweezers to lead to faster breakthroughs in biological research

Jun 17, 2013
A 10 micron crystal placed, using laser light, onto a 50 micron square aperture backed with microfibres ready for freezing and X-ray diffraction studies.

(Phys.org) —A novel process for selecting and examining protein microcrystals, which can be essential for understanding biological functions, is expected to save precious research days and resources and lead to faster breakthroughs in healthcare. Protein microcrystals enable researchers to analyse the structure of molecules and how they behave, for example in disease, but can take a long time to prepare and analyse. A new process for using laser 'tweezers' developed at the Rutherford Appleton Laboratory will help streamline crystal selection. The results are published in Acta Crystallographica D this week.

The technique allows researchers to select and place microscopic protein on customised sample holders for crystallographic analysis on one of beamlines at Diamond , the UK's national synchrotron science facility. Studying through enables researchers to understand the structure and function of a molecule.

The new technique is the result of a cross-campus collaboration between Diamond Light Source and STFC's Central Laser Facility (CLF) and Technology departments. In this area of research, crystals of proteins rather than single molecules must be used, but for many proteins, the crystals formed can be so small (less than 10 microns) that they are very difficult to handle and mount onto standard sample holders for analysis. This can lead to some potentially vital crystals being discarded. STFC's Technology Department helped to overcome this problem by weaving a microfiber web to create a 'net' for the crystals to be mounted on. A laser is then used to grab the minute crystals and move them onto the novel sample holders in the process of laser tweezing.

By using lasers to precisely place these crystals in position, scientists are able to know where to focus the X-ray beam to look at the protein microcrystals. Previously, researchers had had to 'fish' through the sample to load crystals. During this process it was not possible to select and mount individual crystals; it was more of a random approach and needed a significant amount of time to optimise the conditions during the mounting process. Additionally, more time for screening was needed to make sure that the best crystals, e.g. the largest ones, were successfully transferred to the beamline. The use of to streamline the process means precious research days and resources can be saved.

Armin Wagner, project lead at Diamond Light Source, explains why this technique is so important: "Previously we have, in essence, wasted two to three days on the beamline just looking for our best crystals. Now, using the laser tweezers system, we can visually identify and select specific crystals and transfer them to well defined positions on a sample mount rather than relying on a purely random process. Microcrystal work is essential for research in many areas and this collaborative, cross-campus project is addressing problems with crystal supply to allow more efficient research."

Andy Ward at the Central Laser Facility said: "This is a great example of how scientists from different facilities at the Rutherford Appleton Laboratory collaborate to address challenging problems. It's clearly a benefit to have them all on one site here at the Harwell campus".

Explore further: Research team announces new class of compounds that appear to be effective against malaria

add to favorites email to friend print save as pdf

Related Stories

New tool puts LCLS X-ray crystallography on a diet

Oct 30, 2012

A tiny device invented at SLAC National Accelerator Laboratory will make it much easier for scientists to determine the structures of important, delicate proteins by greatly reducing the amount of protein ...

Recommended for you

Molecules that came in handy for first life on Earth

Nov 24, 2014

For the first time, chemists have successfully produced amino acid-like molecules that all have the same 'handedness', from simple building blocks and in a single test tube. Could this be how life started. ...

User comments : 0

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.