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Posted: Mar 14, 2016
'Sweet' quantum dots light the way for new HIV and Ebola treatment
(Nanowerk News) A research team led by the University of Leeds has observed for the first time how HIV and Ebola viruses attach to cells to spread infection.
The findings, published today in the journal Angewandte Chemie ("Compact, Polyvalent Mannose Quantum Dots as Sensitive, Ratiometric FRET Probes for Multivalent Protein-Ligand Interactions"), offer a new way of treating such viruses: instead of destroying the pathogens, introduce a block on how they interact with cells.
Quantum dots are fluorescent crystals in which the color of the emitted light is dependent on the size of the crystal. (Image: Richard E. Cruise, University of Leeds)
Lead author Dr Yuan Guo, from the Astbury Centre for Structural Molecular Biology at the University of Leeds, said: "Until now, how these viruses attach to cells was a 'black box' to chemists. We knew that the viruses were interacting with healthy cells, but the way in which they bound together was still a mystery."
In the study, the researchers used nano-sized crystals (about a millionth of a millimetre in size) called 'quantum dots' that mimicked the shape of the viruses and acted as technological stand-ins in experiments to reveal how they bind to cells.
Quantum dots are fluorescent crystals in which the colour of the emitted light is dependent on the size of the crystal - one of several properties that has led to them becoming the most desirable component for the latest generation of televisions. They have also emerged as an advanced type of fluorescent probe for biomolecular and cellular imaging, making them useful for studying how viruses spread.
Using the fluorescence of the quantum dots, the research team behind the new study were able to illuminate the physical binds that attach them to the cells, also revealing how the viruses would bond.
In order to allow the quantum dots to bind to cells, they first had to be coated in sugar - a new technique that was developed at the University of Leeds for this study.
Study co-author Dr Bruce Turnbull, also from the Astbury Centre, and the University's School of Chemistry, said: "We often only hear about sugar in a negative light, about how consuming it is bad for our health. But there are many different types of sugars that play a vital role in human biology. In fact, all of our cells are coated in sugar and they interact with other cells by proteins binding with these sugars. Indeed, the reason why we have different blood types is because of the different types of sugar coating on our red blood cells.
"Viruses also attach to the surface of healthy cells through interactions between proteins and sugars. These interactions are weak individually, but can be reinforced by forming multiple contacts to offer the viruses a 'way in'. We want to understand what factors control this binding process and, eventually, develop a range of inhibitors designed to target specific viral bindings."
The study has already revealed the different ways in which two cell surface sugar binding proteins that were previously thought to be almost indistinguishable - called 'DC-SIGN' and 'DC-SIGNR' - bind to the HIV and Ebola virus surface sugars, thereby spreading the viruses.
Study co-lead author Dr Dejian Zhou, also from the Astbury Centre and the University's School of Chemistry, said: "These proteins are like twins with different personalities. Their physical make-up is almost identical, yet the efficiency with which they transmit different viruses, such as HIV and Ebola, varies dramatically and the reason behind this had been a mystery.
"Our study has revealed a way to differentiate between these proteins, as we have found that the way in which they bind to virus surface sugars is very different. They both attach via four binding sites to strengthen the bond, but the orientation of these binding pockets differs."
A pioneering tradition in structural biology
Further progress in this area will be boosted by the state-of-the-art facilities in the Astbury Centre, enabling researchers to better understand life in molecular detail.
The University of Leeds has played a key role in the birth of structural biology as a scientific discipline, with the development of X-ray crystallography by Nobel Laureates William and Lawrence Bragg in Leeds in 1912-13.
A recent £17 million investment in some of the best nuclear magnetic resonance and electron microscopy facilities in the world is now enabling scientists to remain at the forefront of research into complex proteins.
A new academic symposium, the Asbury Conversation, is being hosted at the University of Leeds from 11 - 12 April 2016, to bring together leading researchers from across the globe to discuss the most recent innovations, new techniques and technologies in the field of structural molecular biology.
A public exhibition and lecture on Tuesday 12 April follows the symposium, aimed at helping people understand the secret life of molecules, including an exhibit called "The complex life of sugars". Professor Michael Levitt, who was awarded the 2013 Nobel Prize in Chemistry for developing computer-based tools to better understand and predict chemical reactions, will be delivering the talk, "How modelling molecules builds our understanding of life."