For Release: January 10, 2011
Ames, Iowa â€“ Advancements in understanding rotational motion in living cells may help researchers shed light on the causes of deadly diseases, such as Alzheimerâ€™s, according to Ning Fang, an associate scientist at the U.S. Department of Energyâ€™s Ames Laboratory and faculty member at Iowa State University.
In an article entitled â€œResolving Rotational Motions of Nano-objects in Engineered Environments and Live Cells with Gold Nanorods and Differential Interference Contrast Microscopyâ€ published in the November 2 issue of the Journal of the American Chemical Society, and an article in press in ACS Nano, Fang and his research team write about the influence of differential interference contrast Microscopy on revealing nanoparticle movement in living cells.
In the human body, numerous biological nanomachines perform various functions. But according to Fang, scientists have only a limited understanding of how these nanomachines work, especially in cellular environments. And because the malfunction of any of these nanomachines can lead to diseases, such as Alzheimerâ€™s, there is a great need for new techniques to help investigate the composition, dynamics and working mechanisms of these nanomachines.
To understand how these nanomachines work, scientists look at various types of motion in nanomachines that are essential to their function.
(from left) Researchers Ning Fang, Wei Sun and Gufeng Wang.
Translational motion, or movement in which the position of an object is changed, can be tracked through a variety of current techniques. However, rotational motion, which is as important and fundamental as translational motion, was largely unknown due to technical limitations.
Previous techniques, such as particle-tracking or single-molecule fluorescence polarization, only allowed rotational movement to be resolved in vitro, such as in a Petri dish. In their research, Fangâ€™s group has gone beyond studying motions in the in vitro environment to imaging rotational movement in the in vivo, or live cell, environment.
To do this, they rely upon the use of gold nanorods, which are only 25 by 73 nanometers in size (a well-packed bundle of 1000 nanorods has the same diameter as a human hair). In live cells, these non-toxic nanorods scatter light differently depending upon their orientation. Using a technique called differential interference contrast microscopy, or DIC, Fangâ€™s team can capture both the orientation and the position of the gold nanorods in addition to the optical image of the cell and, thus, reveal a particleâ€™s 5D (3 spatial coordinates and 2 orientation angles) movement within living cells.
â€œDIC imagining of this gold nanorod helps give us high angular resolution,â€ says Fang.
â€œThis new technique opens doors to understanding the working mechanism of living nanomachines by revealing their complex internal motions,â€ said Fang. â€œStudying rotational motions at the nanometer scale inside a living cell is just something that has never been done before.â€ He added that understanding this rotational motion is important in the fight against diseases, such as Alzheimerâ€™s, because it can help scientists better understand how neurons are impacted by the environment.
This research was funded by the U.S. Department of Energy Office of Science.
The Ames Laboratory is a U.S. Department of Energy Office of Science research facility operated by Iowa State University. The Ames Laboratory creates innovative materials, technologies and energy solutions. We use our expertise, unique capabilities and interdisciplinary collaborations to solve global problems.
For links to papers go to:
1. Wang, G.; Sun, W.; Luo, Y.; Fang, N.* Resolving Rotational Motions of Nano-objects in Engineered Environments and Live Cells with Gold Nanorod Probes and Differential Interference Contrast Microscopy. Journal of the American Chemical Society, 132 (46), 16417â€“16422 (2010). [Online]
2. A. S. Stender, G. Wang, W. Sun and N. Fang "Influence of Gold Nanorod Geometry on Optical Response" ACS Nano, 2010, 4, 7667-7675. DOI 10.1021/nn102500s [Online]