A
team from the University of Melbourne's Department
of Chemical and Biomolecular Engineering has used
a molecular beacon made from single DNA strands to
measure how easily DNA (e.g. genes) can pass through
the wall of drug delivery particles.
Federation Fellow Professor Frank Caruso, who heads the Centre for Nanoscience
and Nanotechnology, says, “The past number of years has seen major advances in
the design of ‘molecular vehicles' – particles that can be filled with a medicine
or new genes. The vehicles then ferry their contents to the site in the body
where they are needed.”
“One of the major roadblocks that we have encountered in designing these molecular
transport systems is how to get the vehicle contents out of their container once
they reach the site where they are needed.”
In order to achieve this effectively, the researchers need to know how big the
pores in the vehicle's membranes are and how easily the contents can pass through
them. This has proved quite difficult.
Dr Angus Johnston who works with Professor Caruso says, “Scientists designing
these drug-delivery vehicles need to be able to measure the very small number
of molecules which pass through the membrane. Normally, we could label the molecules,
so we can see them as they pass through. The problem with this is that adding
a label alters the size, so the ability to pass through the pore will change
when the label is removed.”
Dr Johnston and Professor Caruso have developed a clever technique that overcomes
this problem which allows scientists to rapidly and accurately determine the
permeability of DNA through films.
The beacons the researchers used are single DNA strands which have a light-emitting
molecule (a fluorophore) at one end and a quencher at the other. A fluorophore
is simply a molecule that emits light and a quencher is a molecule that stops
the fluorophore from emitting light.
The DNA strand self assembles so that the two end segments pair up, forming a
loop in the centre – much like the shape of a round-bottomed flask (see illustration).
This is the closed molecular beacon.
When the beacon is closed the fluorophore on one end of the DNA strand is close
to the “quencher” on the other end, which stops the fluorophore from giving off
light.
To determine the permeability of the capsule, the molecular beacons are placed
inside the delivery vehicle. If DNA passes through the capsule wall, the beacon
opens and the fluorophore emits light. So when DNA passes through the capsule,
the beacon is switched ‘on'. If no DNA passes through the capsule, the beacon
remains switched off.
The researchers used this technique with different length strands of DNA and
were able to use the beacons to successfully determine whether or not the strands
were able to pass through the membrane.
Professor Caruso says, “We hope to now use the technique in the design of intelligent
drug-delivery systems which can transport medicine to target locations and release
the contents in a controlled way.”
The research was recently published in the Journal of the American Chemical Society
and highlighted in the July 15 Issue of the journal Science. This research was
funded by the Australian Research Council.
More information about this article:
Elaine Mulcahy
Media Promotions Officer
emulcahy@unimelb.edu.au
Tel: 61 3 8344 0181
Mob: 0421 641 506
Frank Caruso
Chemical and Biomolecular Engineering
(03) 8344 3461
fcaruso@unimelb.edu.au
Angus Johnston
Chemical and Biomolecular Engineering
(03) 8344 9833
0409 863 255
angusj@unimelb.edu.au
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