Jordan M. Gerton
University of Utah
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Publication
Featured researches published by Jordan M. Gerton.
Nature | 2000
Jordan M. Gerton; Dmitry Strekalov; Ionut D. Prodan; Randall G. Hulet
Quantum theory predicts that Bose–Einstein condensation of a spatially homogeneous gas with attractive interactions is precluded by a conventional phase transition into either a liquid or solid. When confined to a trap, however, such a condensate can form, provided that its occupation number does not exceed a limiting value. The stability limit is determined by a balance between the self-attractive forces and a repulsion that arises from position–momentum uncertainty under conditions of spatial confinement. Near the stability limit, self-attraction can overwhelm the repulsion, causing the condensate to collapse. Growth of the condensate is therefore punctuated by intermittent collapses that are triggered by either macroscopic quantum tunnelling or thermal fluctuation. Previous observations of growth and collapse dynamics have been hampered by the stochastic nature of these mechanisms. Here we report direct observations of the growth and subsequent collapse of a 7Li condensate with attractive interactions, using phase-contrast imaging. The success of the measurement lies in our ability to reduce the stochasticity in the dynamics by controlling the initial number of condensate atoms using a two-photon transition to a diatomic molecular state.
Nano Letters | 2010
Eyal Shafran; Benjamin D. Mangum; Jordan M. Gerton
Precision measurements of resonant energy transfer from isolated quantum dots (QDs) to individual carbon nanotubes (CNTs) exhibit unique features due to the one-dimensional nature of CNTs. In particular, excitons can be created at varying distances from the QD at different locations along the CNT length. This leads to large variations in energy transfer length scales for different QDs and a novel saturation of the energy transfer efficiency at ∼96%, seemingly independent of CNT chirality.
Applied Physics Letters | 2006
Changan Xie; Chun Mu; Jonathan R. Cox; Jordan M. Gerton
High-density samples of fluorescent quantum dots (QDs) were imaged using an apertureless near-field optical microscopy technique. QD fluorescence was modulated by oscillating a silicon atomic force microscope tip above an illuminated sample and a lock-in amplifier was used to suppress background from the excitation laser. Spatial resolution near 10nm and a peak signal-to-noise ratio (SNR) of ∼60 were achieved. Individual QDs within high-density ensembles were still easily resolved (SNR>5) at a density of 14QDs∕μm2. These results have favorable implications for the eventual nanoscale imaging of viable biological systems, such as cellular membranes.
Physical Review A | 2001
Jordan M. Gerton; Brian J. Frew; Randall G. Hulet
A light-induced frequency shift is observed in single-photon photoassociative spectra of magnetically trapped, quantum degenerate
Optics Express | 2008
Benjamin D. Mangum; Chun Mu; Jordan M. Gerton
{}^{7}\mathrm{Li}.
Biochemical and Biophysical Research Communications | 2013
Jeffery Hodges; Xiaolin Tang; Michael B. Landesman; John B. Ruedas; Anil Ghimire; Manasa V. Gudheti; Jacques Perrault; Erik M. Jorgensen; Jordan M. Gerton; Saveez Saffarian
The shift is a manifestation of the coupling between the threshold continuum scattering states and discrete bound levels in the excited-state molecular potential induced by the photoassociation laser. The frequency shift is observed to be linear in the laser intensity with a measured proportionality constant that is in good agreement with theoretical predictions. This phenomenon has important implications for a scheme to alter the interactions between atoms in a Bose-Einstein condensate using photoassociation resonances.
Nano Letters | 2009
Benjamin D. Mangum; Eyal Shafran; Chun Mu; Jordan M. Gerton
We investigate the limits of one-photon fluorescence as a contrast mechanism in nanoscale-resolution tip-enhanced optical microscopy. Specifically, we examine the magnitude of tip-induced signal enhancement needed to resolve individual fluorophores within densely-packed ensembles. Modulation of fluorescence signals induced by an oscillating tip followed by demodulation with a lock-in amplifier increases image contrast by nearly two orders of magnitude. A theoretical model of this simple modulation/ demodulation scheme predicts an optimal value for the tip-oscillation amplitude that agrees with experimental measurements. Further, as an important step toward the eventual application of tip-enhanced fluorescence microscopy to the nanoscale structural analysis of biomolecular systems, we show that requisite signal enhancement factors are within the capabilities of commercially available silicon tips.
Biomedical Optics Express | 2014
Tali Ilovitsh; Amihai Meiri; Carl G. Ebeling; Rajesh Menon; Jordan M. Gerton; Erik M. Jorgensen; Zeev Zalevsky
Vesicular stomatitis virus (VSV) is a prototypic negative sense single-stranded RNA virus. The bullet-shape appearance of the virion results from tightly wound helical turns of the nucleoprotein encapsidated RNA template (N-RNA) around a central cavity. Transcription and replication require polymerase complexes, which include a catalytic subunit L and a template-binding subunit P. L and P are inferred to be in the cavity, however lacking direct observation, their exact position has remained unclear. Using super-resolution fluorescence imaging and atomic force microscopy (AFM) on single VSV virions, we show that L and P are packaged asymmetrically towards the blunt end of the virus. The number of L and P proteins varies between individual virions and they occupy 57 ± 12 nm of the 150 nm central cavity of the virus. Our finding positions the polymerases at the opposite end of the genome with respect to the only transcriptional promoter.
Scientific Reports | 2015
Anil Ghimire; Eyal Shafran; Jordan M. Gerton
We demonstrate a near-field tomography method for investigating the coupling between a nanoscopic probe and a fluorescent sample. By correlating the arrival of single fluorescence photons with the lateral and vertical position of an oscillating tip, a complete three-dimensional analysis of the near-field coupling is achieved. The technique is used to reveal a number of interesting three-dimensional near-field features and to improve image contrast in tip-enhanced fluorescence microscopy.
Physical Review B | 2012
Hyunjeong Kim; Anil Ghimire; Shirin Jamali; Thaddee K. Djidjou; Jordan M. Gerton; Andrey Rogachev
Localization of a single fluorescent particle with sub-diffraction-limit accuracy is a key merit in localization microscopy. Existing methods such as photoactivated localization microscopy (PALM) and stochastic optical reconstruction microscopy (STORM) achieve localization accuracies of single emitters that can reach an order of magnitude lower than the conventional resolving capabilities of optical microscopy. However, these techniques require a sparse distribution of simultaneously activated fluorophores in the field of view, resulting in larger time needed for the construction of the full image. In this paper we present the use of a nonlinear image decomposition algorithm termed K-factor, which reduces an image into a nonlinear set of contrast-ordered decompositions whose joint product reassembles the original image. The K-factor technique, when implemented on raw data prior to localization, can improve the localization accuracy of standard existing methods, and also enable the localization of overlapping particles, allowing the use of increased fluorophore activation density, and thereby increased data collection speed. Numerical simulations of fluorescence data with random probe positions, and especially at high densities of activated fluorophores, demonstrate an improvement of up to 85% in the localization precision compared to single fitting techniques. Implementing the proposed concept on experimental data of cellular structures yielded a 37% improvement in resolution for the same super-resolution image acquisition time, and a decrease of 42% in the collection time of super-resolution data with the same resolution.