DNA-wrapped carbon nanotubes serve as sensors in living cells
James E. Kloeppel, Physical Sciences Editor
CHAMPAIGN, Ill. — Single walled carbon nanotubes wrapped with DNA can be placed inside living cells and detect trace amounts of harmful contaminants using near infrared light, report researchers at the University of Illinois at Urbana-Champaign. Their discovery opens the door to new types of optical sensors and biomarkers that exploit the unique properties of nanoparticles in living systems.
“This is the first nanotube-based sensor that can detect analytes at the subcellular level,” said Michael Strano, a professor of chemical and biomolecular engineering at Illinois and corresponding author of a paper to appear in the Jan. 27 issue of the journal Science. “We also show for the first time that a subtle rearrangement of an adsorbed biomolecule can be directly detected by a carbon nanotube.”
At the heart of the new detection system is the transition of DNA secondary structure from the native, right-handed “B” form to the alternate, left-handed “Z” form.
“We found that the thermodynamics that drive the switching back and forth between these two forms of DNA structure would modulate the electronic structure and optical emission of the carbon nanotube,” said Strano, who is also a researcher at the Beckman Institute for Advanced Science and Technology and at the university’s Micro and Nanotechnology Laboratory.
To make their sensors, the researchers begin by wrapping a piece of double-stranded DNA around the surface of a single-walled carbon nanotube, in much the same fashion as a telephone cord wraps around a pencil. The DNA starts out wrapping around the nanotube with a certain shape that is defined by the negative charges along its backbone.
When the DNA is exposed to ions of certain atoms – such as calcium, mercury and sodium – the negative charges become neutralized and the DNA changes shape in a similar manner to its natural shape-shift from the B form to Z form. This reduces the surface area covered by the DNA, perturbing the electronic structure and shifting the nanotube’s natural, near infrared fluorescence to a lower energy.
“The change in emission energy indicates how many ions bind to the DNA,” said graduate student Daniel Heller, lead author of the Science paper. “Removing the ions will return the emission energy to its initial value and flip the DNA back to the starting form, making the process reversible and reusable.”
The researchers demonstrated the viability of their measurement technique by detecting low concentrations of mercury ions in whole blood, opaque solutions, and living mammalian cells and tissues – examples where optical sensing is usually poor or ineffective. Because the signal is in the near infrared, a property unique to only a handful of materials, it is not obscured by the natural fluorescence of polymers and living tissues.
“The nanotube surface acts as the sensor by detecting the shape change of the DNA as it responds to the presence of target ions,” Heller said.
Co-authors of the paper with Strano and Heller are graduate student Esther Jeng and undergraduate students Tsun-Kwan Yeung, Brittany Martinez, Anthonie Moll and Joseph Gastala. The work was funded by the National Science Foundation.
Optical Detection of DNA Conformational Polymorphism on Single-Walled Carbon Nanotubes
Science 27 January 2006:
Vol. 311. no. 5760, pp. 508 – 511
Daniel A. Heller,1 Esther S. Jeng,2 Tsun-Kwan Yeung,2 Brittany M. Martinez,2 Anthonie E. Moll,2 Joseph B. Gastala,2 Michael S. Strano2*
The transition of DNA secondary structure from an
analogous B to Z conformation modulates the dielectric environment of the single-walled carbon nanotube (SWNT) around which it is adsorbed. The SWNT band-gap fluorescence undergoes a red shift when an encapsulating 30-nucleotide oligomer is exposed to counter ions that screen the charged backbone. The transition is thermodynamically identical for DNA on and off the nanotube, except that the propagation length of the former is shorter by five-sixths. The magnitude of the energy shift is described by using an effective medium model and the DNA geometry on the nanotube sidewall. We demonstrate the detection of the B-Z change in whole blood, tissue, and from within living mammalian cells.
1 Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
2 Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.