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Using Carbon Nanotubes To Seek and Destroy Anthrax Toxin and Other Harmful Proteins
New technology could enable new cancer treatment
techniques and antibacterial coatings
Troy, N.Y. — Researchers at Rensselaer Polytechnic Institute
have developed a new way to seek out specific proteins,
including dangerous proteins such as anthrax toxin, and render
them harmless using nothing but light. The technique lends
itself to the creation of new antibacterial and antimicrobial
films to help curb the spread of germs, and also holds promise
for new methods of seeking out and killing tumors in the human
body.
Scientists have long been interested in wrapping proteins
around carbon nanotubes, and the process is used for various
applications in imaging, biosensing, and cellular delivery. But
this new study at Rensselaer is the first to remotely control
the activity of these conjugated nanotubes. Details of the
project are outlined in the article “Nanotube-Assisted Protein
Deactivation” in the December issue of Nature
Nanotechnology.
A team of Rensselaer researchers led by Ravi S. Kane,
professor of chemical and biological engineering, has worked
for nearly a year to develop a means to remotely deactivate
protein-wrapped carbon nanotubes by exposing them to invisible
and near-infrared light. The group demonstrated this method by
successfully deactivating anthrax toxin and other proteins.
“By attaching peptides to carbon nanotubes, we gave them the
ability to selectively recognize a protein of interest — in
this case anthrax toxin — from a mixture of different
proteins,” Kane said. “Then, by exposing the mixture to light,
we could selectively deactivate this protein without disturbing
the other proteins in the mixture.”
By conjugating carbon nanotubes with different peptides,
this process can be easily tailored to work on other harmful
proteins, Kane said. Also, employing different wavelengths of
light that can pass harmlessly through the human body, the
remote control process will also be able to target and
deactivate specific proteins or toxins in the human body.
Shining light on the conjugated carbon nanotubes creates free
radicals, called reactive oxygen species. It was the presence
of radicals, Kane said, that deactivated the proteins.
Kane’s new method for selective nanotube-assisted protein
deactivation could be used in defense, homeland security, and
laboratory settings to destroy harmful toxins and pathogens.
The method could also offer a new method for the targeted
destruction of tumor cells. By conjugating carbon nanotubes
with peptides engineered to seek out specific cancer cells, and
then releasing those nanotubes into a patient, doctors may be
able to use this remote protein deactivation technology as a
powerful tool to prevent the spread of cancer.
Kane’s team also developed a thin, clear film made of carbon
nanotubes that employs this technology. This self-cleaning film
may be fashioned into a coating that — at the flip of a light
switch — could help prevent the spread of harmful bacteria,
toxins, and microbes.
“The ability of these coatings to generate reactive oxygen
species upon exposure to light might allow these coatings to
kill any bacteria that have attached to them,” Kane said. “You
could use these transparent coatings on countertops, doorknobs,
in hospitals or airplanes — essentially any surface, inside or
outside, that might be exposed to harmful contaminants.”
Kane said he and his team will continue to hone this new
technology and further explore its potential applications.
Co-authors of the paper include Department of Chemical and
Biological Engineering graduate students Amit Joshi and Shyam
Sundhar Bale; postdoctoral researcher Supriya Punyani;
Rensselaer Nanotechnology Center Laboratory Manager Hoichang
Yang; and professor Theodorian Borca-Tasciuc of the Department
of Mechanical, Aerospace, and Nuclear Engineering.
The group has filed a patent disclosure for their new
selective nanotube-assisted protein deactivation technology.
The research project was funded by the U.S. National Institutes
of Health and the National Science Foundation.
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Published
December 9,
2007 |
Contact: Michael Mullaney
Phone: (518) 276-6161
E-mail: mullam@rpi.edu |
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