How do the power plants of the cell—the mitochondria—use their defence mechanisms to fight diseases such as Parkinson’s disease? This debilitating disorder is caused by an accumulation of proteins that have folded incorrectly.
The misfolded proteins then clump together and form sticky, cell-damaging deposits called plaques.
“We know that mitochondria are at the centre of the aging process,” says Prof Nick Hoogenraad, executive director of the La Trobe Institute for Molecular Science (LIMS). Nick and his team have found a mechanism mitochondria use to remove the plaques that are prone to form as we age.
A Parkinson patient who can walk again, and improved life for people with the behavioural disorder known as Tourette syndrome.
These are two of the results of a partnership between University of Queensland neurologist Prof Peter Silburn and neurosurgeon Dr Terry Coyne who have ventured deeper into the human brain than anyone else in the world.
Peter treats patients at St. Andrew’s Hospital in Brisbane using deep brain stimulation, a technique that uses electrodes to stimulate a region some 12 centimetres under the surface of the brain.
“There are 100 billion neurons in the brain and we can’t restore all of them. But the deep brain is like a telephone exchange—by stimulating this one section of the brain, you can unblock the flow of messages,” Peter says. Continue reading Parkinson answers deep in the brain→
What began decades ago as the discovery of an antibody from mice that targets human cancer cells is now undergoing human trials in the US as the basis of a treatment for acute leukaemia.
The antibody targets a protein called EphA3, which is found in about half of all acute leukaemias as well as many other human cancers including a significant proportion of malignant melanomas, brain tumours and lung cancers. The antibody, called KB004, has been shown to kill certain types of cancerous tumours grown from human samples. Continue reading Life’s work closer to saving lives→
A Flinders University chemist is using Australia’s OPAL research reactor at Lucas Heights in Sydney to investigate ancient Aboriginal Australian society.
Using the technique called neutron activation analysis, Dr Rachel Popelka-Filcoff can “geochemically fingerprint” Aboriginal ochre pigments from different locations, archaeological sites and artefacts.
As the geochemical composition of ochre varies with location, she can correlate each sample with its site of origin, gaining information on cultural practices, travel and exchange patterns, and the relationship of Aboriginal people to the landscape. “Ochre pigments are highly significant in Aboriginal culture,” says Rachel. “Cultural expression often requires a specific pigment. Applying ochre to an object such as a spear can transform both its colour and its cultural meaning.”
Dr Roman Dronov, also from Flinders, is using the reactor to study the formation of bacterial protein layers. He is applying what he finds to constructing a new type of biosensor based on these layers and porous silicon. These highly sensitive devices can rapidly detect trace amounts of molecules, such as environmental poisons and markers of disease—a great improvement on traditional analytical methods. Continue reading OPAL reactor fingerprints Aboriginal ochre→
Donor corneas conditioned with DNA before being transplanted into new eyes are already actively contributing to their own success in experimental animals such as sheep.
The DNA is inserted into the cells of the cornea after it has been harvested. Then, following implantation, it produces proteins that help overcome immunological rejection.
This is one of many strands of research aimed at increasing the success rates of corneal transplants and other eye disease treatments undertaken by Prof Keryn Williams at Flinders University. Continue reading Helping eyes to help themselves→
An Australian invention is making it cheaper, quicker and safer to manufacture the radioactive tracers used in latest medical imaging techniques to track down increasingly smaller clusters of cancer cells.
Like preparing a cake in a mixing bowl, the chemical reactions to make the tracers involve putting the ingredients together in the right proportions. The next generation of tracers can have a more complex recipe—and so can be more difficult to produce using just one ‘mixing bowl’ at a time. Continue reading Two steps forward for cancer detection→
There’s a new diagnostic tool being developed to target melanoma, the deadly form of skin cancer with which more than 10,000 Australians are diagnosed each year.
It’s a chemical compound designed to highlight small traces of these cancer cells in the body.
Melanoma occurs when the cells that make melanin, the dark pigment normally found in the skin, become cancerous. Melanoma cells often spread elsewhere in the body before the primary tumours are detected and removed surgically. Clusters of these melanoma cells can be hard to detect before they grow into tumours by which time they are often incurable. Continue reading Unmasking melanoma early→
Four of Australia’s most accomplished scientists have been elected to the oldest scientific academy in continuous existence, the Royal Society of London.
Prof Ian Frazer, Prof Alan Cowman, Prof Mark Randolph and Dr Patrick Tam join 40 other scientists to be elected to the Royal Society in 2011, which celebrated its 350th anniversary last year.
Australian researchers have invented a small, smart, self-managed hearing aid that outperforms most conventional hearing aids for less than half the price.
It uses technology first developed for Australia’s bionic ear, and is so simple to set up that most users can buy one over the internet and fit it themselves.
That brings the cost down to between $1,000 and $1,500, or less than $3,000 for a pair.
Some of the biochemical tricks the malaria parasite uses to become resistant have been unravelled thanks to a series of discoveries by Dr Rowena Martin and her colleagues at the Australian National University.
She is using those insights to give a new lease of life to chloroquine, the wonder drug against malaria first discovered in the 1950s.
For more than half a century chloroquine saved hundreds of millions of lives, but now chloroquine-resistant malaria strains have become common in developing countries.
Rowena is working to understand what happened. The single-celled malaria parasite enters our bodies when we are bitten by an infected mosquito.
It eventually invades and plunders our red blood cells, consuming the haemoglobin contained within.
The digestion of haemoglobin, which takes place in the parasite’s stomach compartment, releases the iron-containing, nonprotein component, haem.
Free haem is toxic to the parasite, which responds by converting it to a harmless crystal. Chloroquine works by blocking the formation of these crystals.
Ten years ago researchers discovered that just a few small changes in a protein PfCRT were enough to give the parasite resistance to chloroquine. But they did not know what the changes did.
Rowena developed a system to study PfCRT in frog eggs—allowing her to examine it in isolation and in detail.
“We found that it moves chloroquine out of the parasite’s stomach compartment so that the drug can’t accumulate at its site of action.” For her achievements to date, in 2010 Rowena won a $20,000 L’Oréal Australia For Women in Science Fellowship.
Photo: Rowena Martin, the Australian National University, Canberra/The University of Melbourne. Credit: L’oréal Australia/SDP media.
Research School of Biology, The Australian National University, Rowena Martin, Tel: +61 2 6125 8589, Rowena.Martin@anu.edu.au, www.scienceinpublic.com.au/loreal
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