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      Using fixed fiduciary markers for stage drift correction

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          Abstract

          To measure nanometric features with super-resolution requires that the stage, which holds the sample, be stable to nanometric precision. Herein we introduce a new method that uses conventional equipment, is low cost, and does not require intensive computation. Fiduciary markers of approximately 1 µm x 1 µm x 1 µm in x, y, and z dimensions are placed at regular intervals on the coverslip. These fiduciary markers are easy to put down, are completely stationary with respect to the coverslip, are bio-compatible, and do not interfere with fluorescence or intensity measurements. As the coverslip undergoes drift (or is purposely moved), the x-y center of the fiduciary markers can be readily tracked to 1 nanometer using a Gaussian fit. By focusing the light slightly out-of-focus, the z-axis can also be tracked to < 5 nm for dry samples and <17 nm for wet samples by looking at the diffraction rings. The process of tracking the fiduciary markers does not interfere with visible fluorescence because an infrared light emitting diode (IR-LED) (690 and 850 nm) is used, and the IR-light is separately detected using an inexpensive camera. The resulting motion of the coverslip can then be corrected for, either after-the-fact, or by using active stabilizers, to correct for the motion. We applied this method to watch kinesin walking with ≈8 nm steps.

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          Most cited references20

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          Far-field optical nanoscopy.

          In 1873, Ernst Abbe discovered what was to become a well-known paradigm: the inability of a lens-based optical microscope to discern details that are closer together than half of the wavelength of light. However, for its most popular imaging mode, fluorescence microscopy, the diffraction barrier is crumbling. Here, I discuss the physical concepts that have pushed fluorescence microscopy to the nanoscale, once the prerogative of electron and scanning probe microscopes. Initial applications indicate that emergent far-field optical nanoscopy will have a strong impact in the life sciences and in other areas benefiting from nanoscale visualization.
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            Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution.

            Contrary to the well known diffraction limit, the fluorescence microscope is in principle capable of unlimited resolution. The necessary elements are spatially structured illumination light and a nonlinear dependence of the fluorescence emission rate on the illumination intensity. As an example of this concept, this article experimentally demonstrates saturated structured-illumination microscopy, a recently proposed method in which the nonlinearity arises from saturation of the excited state. This method can be used in a simple, wide-field (nonscanning) microscope, uses only a single, inexpensive laser, and requires no unusual photophysical properties of the fluorophore. The practical resolving power is determined by the signal-to-noise ratio, which in turn is limited by photobleaching. Experimental results show that a 2D point resolution of <50 nm is possible on sufficiently bright and photostable samples.
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              Upconversion nanoparticles in biological labeling, imaging, and therapy.

              Upconversion refers to non-linear optical processes that convert two or more low-energy pump photons to a higher-energy output photon. After being recognized in the mid-1960s, upconversion has attracted significant research interest for its applications in optical devices such as infrared quantum counter detectors and compact solid-state lasers. Over the past decade, upconversion has become more prominent in biological sciences as the preparation of high-quality lanthanide-doped nanoparticles has become increasingly routine. Owing to their small physical dimensions and biocompatibility, upconversion nanoparticles can be easily coupled to proteins or other biological macromolecular systems and used in a variety of assay formats ranging from bio-detection to cancer therapy. In addition, intense visible emission from these nanoparticles under near-infrared excitation, which is less harmful to biological samples and has greater sample penetration depths than conventional ultraviolet excitation, enhances their prospects as luminescent stains in bio-imaging. In this article, we review recent developments in optical biolabeling and bio-imaging involving upconversion nanoparticles, simultaneously bringing to the forefront the desirable characteristics, strengths and weaknesses of these luminescent nanomaterials.
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                Author and article information

                Journal
                Opt Express
                Opt Express
                OE
                Optics Express
                Optical Society of America
                1094-4087
                14 May 2012
                24 May 2012
                21 May 2012
                14 May 2013
                : 20
                : 11
                : 12177-12183
                Affiliations
                [1 ]Department of Physics, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA
                [2 ]Biophysics program, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA
                [3 ]Center for Physics in Living Cells, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA
                Author notes
                Article
                164559
                10.1364/OE.20.012177
                3482917
                22714205
                c1053186-12d5-40f3-a1a9-35e49a66c1ca
                ©2012 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 12 March 2012
                : 7 May 2012
                : 7 May 2012
                Funding
                Funded by: NIH
                Award ID: GM068625
                Funded by: NSF
                Award ID: DBI- 02-15869
                Award ID: EAGER 0968976
                Award ID: 082265
                Categories
                Research-Article
                Custom metadata
                True
                12

                Ophthalmology & Optometry
                (110.0180) microscopy,(180.2520) fluorescence microscopy
                Ophthalmology & Optometry
                (110.0180) microscopy, (180.2520) fluorescence microscopy

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