Megan M. Spence
University of California, Berkeley
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Publication
Featured researches published by Megan M. Spence.
Proceedings of the National Academy of Sciences of the United States of America | 2001
Megan M. Spence; Seth M. Rubin; Ivan E. Dimitrov; E. Janette Ruiz; David E. Wemmer; Alexander Pines; Shao Qin Yao; Feng Tian; Peter G. Schultz
The detection of biological molecules and their interactions is a significant component of modern biomedical research. In current biosensor technologies, simultaneous detection is limited to a small number of analytes by the spectral overlap of their signals. We have developed an NMR-based xenon biosensor that capitalizes on the enhanced signal-to-noise, spectral simplicity, and chemical-shift sensitivity of laser-polarized xenon to detect specific biomolecules at the level of tens of nanomoles. We present results using xenon “functionalized” by a biotin-modified supramolecular cage to detect biotin–avidin binding. This biosensor methodology can be extended to a multiplexing assay for multiple analytes.
Proceedings of the National Academy of Sciences of the United States of America | 2003
Adam J. Moulé; Megan M. Spence; Song-I Han; Juliette A. Seeley; Kimberly L. Pierce; Sunil Saxena; Alexander Pines
A technique is proposed in which an NMR spectrum or MRI is encoded and stored as spin polarization and is then moved to a different physical location to be detected. Remote detection allows the separate optimization of the encoding and detection steps, permitting the independent choice of experimental conditions and excitation and detection methodologies. In the initial experimental demonstration of this technique, we show that taking dilute 129Xe from a porous sample placed inside a large encoding coil and concentrating it into a smaller detection coil can amplify NMR signal. In general, the study of NMR active molecules at low concentration that have low physical filling factor is facilitated by remote detection. In the second experimental demonstration, MRI information encoded in a very low-field magnet (4–7 mT) is transferred to a high-field magnet (4.2 T) to be detected under optimized conditions. Furthermore, remote detection allows the utilization of ultrasensitive optical or superconducting quantum interference device detection techniques, which broadens the horizon of NMR experimentation.
Archive | 2002
Alexander Pines; John W. Logan; Megan M. Spence
By means of optical pumping with laser light, the nuclear spin polarization of gaseous xenon can be enhanced by many orders of magnitude. The enhanced polarization has allowed an extension of the pioneering experiments of Fraissard and coworkers to novel applications of NMR and MRI in chemistry, materials science and biomedicine. Examples are presented of developments and applications of laser-polarized xenon NMR and MRI on distance scales from nanometers to meters. The size of the xenon atom is similar to that of small organic molecules, such as methane, yet the nuclear magnetic resonance (NMR) signal from xenon proves a more sensitive probe for the local environment. Laser-polarized xenon NMR has been used, in collaboration with Sozzani and coworkers, to investigate the interactions present in an effectively one- dimensional gas phase inside nanochannels. Small changes in channel size and/or structure lead to very different modes of diffusion. Optically pumped Xe NMR can distinguish between these different diffusion modes out to unparalleled time scales (several tens of seconds). These studies are particularly useful for gaining a fundamental understanding of the laws that govern heterogenous mass transport such as gas transport into porous catalysts or molecular sieves, or liquid transport through pore-forming transmembrane proteins in biological systems. The understanding of mass transport inside microporous materials is crucial for many industrial and commercial processes. Recent experiments will also be described in which xenon has been used to investigate the cavities of biological nanosystems and in which polarization has been transferred to molecules on surfaces and in solution. As an example, in collaboration with Wemmer and coworkers, xenon has been used as a molecular probe to investigate the hydrophobic surfaces and interiors of macrocyclic molecules and proteins; recent results show evidence for binding of xenon to the outside of a protein, a proposed cause of the anesthetic mechanism of xenon. Indeed, localized injection of polarized xenon solutions into human blood has provided observations of the real-time process of xenon penetrating red blood cells. The injection technique also makes it possible to provide enhanced magnetic resonance images of localized areas in living organisms. Furthermore, the use of laser-polarized xenon also opens an exciting new frontier in the possibility of “functionalized xenon” as a biosensor of analytes and metabolites in chemistry, materials science and biomedicine. The novel biosensor offers advantages of multiplexing capabilities and the possibility of detection in-vivo.
Journal of the American Chemical Society | 2004
Megan M. Spence; E. Janette Ruiz; Seth M. Rubin; Thomas J. Lowery; Nicolas Winssinger; Peter G. Schultz; David E. Wemmer; Alexander Pines
Proceedings of the National Academy of Sciences of the United States of America | 2000
Seth M. Rubin; Megan M. Spence; Boyd M. Goodson; David E. Wemmer; Alexander Pines
Journal of Magnetic Resonance | 2001
Seth M. Rubin; Megan M. Spence; Alexander Pines; David E. Wemmer
Journal of the American Chemical Society | 2001
Seth M. Rubin; Megan M. Spence; Ivan E. Dimitrov; E. Janette Ruiz; and Alexander Pines; David E. Wemmer
Archive | 2002
Alexander Pines; Sunil Saxena; Adam J. Moulé; Megan M. Spence; Juliette A. Seeley; Kimberly Pierce; Song-I Han; Josef Granwehr
Magnetic Resonance Imaging | 2003
Thomas J. Lowery; Seth M. Rubin; E. Janette Ruiz; Megan M. Spence; Nicolas Winssinger; Peter G. Schultz; Alexander Pines; David E. Wemmer
Archive | 2001
Alexander Pines; David E. Wemmer; Megan M. Spence; Seth M. Rubin