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Posted: February 5, 2007
Bright nanoparticles aid basic cancer biology studies
(Nanowerk News) Though there is little doubt that nanoscale devices are going to play a critical role in improving cancer detection and treatment over the next five to ten years, nanoparticles are already having a major impact on the way that cancer biologists study the processes that go awry within malignant and metastatic cells. By taking advantage of the unique optical and other physical properties of nanoscale materials, researchers have created a veritable toolbox of nanoparticle probes that can track the fate of cells and even individual molecules in complex environments, opening the door to a wide range of new experiments designed to better understand the cancer process.
These new quantum dots are made by adding small amounts of manganese to the zinc sulfide and zinc selenide used to form the fluorescent nanocrystals. Adding a 2-3 atom-thick layer of zinc selenide to the outside of these quantum dots enabled the researchers to add a thin coating for sulfur-containing molecules that render the nanoparticles soluble in water without adversely affecting the nanoparticles’ bright fluorescent emissions.
The sulfur groups also provide a site for attaching targeting molecules and other biochemical probes useful in cell biology studies. In this paper, the researchers showed that they could attach the biomolecule avidine to the nanocrystals and use it to visualize the molecule biotin, to which avidine binds tightly. The researchers note that as with conventional cadmium-based quantum dots, they can tune the optical properties of these quantum dots by changing the chemical conditions used to make these nanoparticles.
In another paper published in Nano Letters ("Semiconductor Quantum Rods as Single Molecule Fluorescent Biological Labels"), A. Paul Alivisatos, Ph.D., and colleagues at the University of California, Berkeley, and the Lawrence Berkeley National Laboratory, describe their development of quantum rods that are even brighter than spherical quantum dots. The rods, which range from 2 to 10 nanometers in diameter and 5 to 100 nanometers in length, can serve as molecule-sized labels for biological research whose color is determined by the exact dimensions of a particular quantum rod.
In their native form, quantum rods are relatively inert and insoluble in water, making it difficult to modify them with biological targeting agents and use them as biological labels. Alivisatos and his collaborators solved this problem by depositing a thin film of a silicon-containing compound known as a silane. The investigators then showed that the resulting silane-coated quantum rods, which were stable in water for over two years, were biocompatible, water-soluble, and easily modified with targeting agents.
In one experiment, the investigators labeled a quantum rod with a monoclonal antibody that recognizes the breast cancer biomarker known as HER2 and used it to detect HER2 on the surface of cultured HER2-positive breast cancer cells. In another experiment, the investigators were able to track individual quantum rods as they traversed the inside of a cultured breast cancer cell.
Lounis and his collaborators were interested specifically in designing a nanoprobe for tracking molecular motion in the normally fluid cell membrane without interfering with normal membrane function. To track the gold nanoparticles, the researchers used a technique called photothermal spectroscopy, which can detect the small amount of heat that gold nanoparticles emit when irradiated with light. This measurement technique, which the investigators refined for use with gold nanoparticles, enabled the unprecedented detection of individual 1.4-nanometer gold particles in live cells. Furthermore, they were able to make video recordings of the nanoparticles attached to individual proteins in the cell membrane.
Source: National Cancer Institute
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