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      Fluorescent Probes and Fluorescence (Microscopy) Techniques — Illuminating Biological and Biomedical Research

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          Abstract

          Fluorescence, the absorption and re-emission of photons with longer wavelengths, is one of those amazing phenomena of Nature. Its discovery and utilization had, and still has, a major impact on biological and biomedical research, since it enables researchers not just to visualize normal physiological processes with high temporal and spatial resolution, to detect multiple signals concomitantly, to track single molecules in vivo, to replace radioactive assays when possible, but also to shed light on many pathobiological processes underpinning disease states, which would otherwise not be possible. Compounds that exhibit fluorescence are commonly called fluorochromes or fluorophores and one of these fluorescent molecules in particular has significantly enabled life science research to gain new insights in virtually all its sub-disciplines: Green Fluorescent Protein. Because fluorescent proteins are synthesized in vivo, integration of fluorescent detection methods into the biological system via genetic techniques now became feasible. Currently fluorescent proteins are available that virtually span the whole electromagnetic spectrum. Concomitantly, fluorescence imaging techniques were developed, and often progress in one field fueled innovation in the other. Impressively, the properties of fluorescence were utilized to develop new assays and imaging modalities, ranging from energy transfer to image molecular interactions to imaging beyond the diffraction limit with super-resolution microscopy. Here, an overview is provided of recent developments in both fluorescence imaging and fluorochrome engineering, which together constitute the “fluorescence toolbox” in life science research.

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          Most cited references65

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          The green fluorescent protein.

          R Tsien (1998)
          In just three years, the green fluorescent protein (GFP) from the jellyfish Aequorea victoria has vaulted from obscurity to become one of the most widely studied and exploited proteins in biochemistry and cell biology. Its amazing ability to generate a highly visible, efficiently emitting internal fluorophore is both intrinsically fascinating and tremendously valuable. High-resolution crystal structures of GFP offer unprecedented opportunities to understand and manipulate the relation between protein structure and spectroscopic function. GFP has become well established as a marker of gene expression and protein targeting in intact cells and organisms. Mutagenesis and engineering of GFP into chimeric proteins are opening new vistas in physiological indicators, biosensors, and photochemical memories.
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            Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy.

            Recent advances in far-field fluorescence microscopy have led to substantial improvements in image resolution, achieving a near-molecular resolution of 20 to 30 nanometers in the two lateral dimensions. Three-dimensional (3D) nanoscale-resolution imaging, however, remains a challenge. We demonstrated 3D stochastic optical reconstruction microscopy (STORM) by using optical astigmatism to determine both axial and lateral positions of individual fluorophores with nanometer accuracy. Iterative, stochastic activation of photoswitchable probes enables high-precision 3D localization of each probe, and thus the construction of a 3D image, without scanning the sample. Using this approach, we achieved an image resolution of 20 to 30 nanometers in the lateral dimensions and 50 to 60 nanometers in the axial dimension. This development allowed us to resolve the 3D morphology of nanoscopic cellular structures.
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              Two-photon laser scanning fluorescence microscopy

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                28 November 2012
                December 2012
                : 17
                : 12
                : 14067-14090
                Affiliations
                Bionanoscience and Bio-Imaging Program, Cellular Stress and Ageing Program, BIO&NANO-SOLUTIONS, Helmutstr. 3A, D-40472, Düsseldorf, Germany; Email: gpcdrummen@ 123456bionano-solutions.de ; Tel.: +49-211-2297-3648; Fax: +49-3222-240-7500
                Article
                molecules-17-14067
                10.3390/molecules171214067
                6268024
                23192185
                d884ca3a-8997-4442-b205-15825c9857e9
                © 2012 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 23 November 2012
                : 26 November 2012
                : 26 November 2012
                Categories
                Editorial

                fluorescence,fluorescence microscopy,fluorochrome,dye,probe,super-resolution,dstorm,fret,frap,quenching,twisted intramolecular charge transfer,excimer,photoswitching,fluorescent protein,phthalocyanines,pyrene,lithium,quantum dot,fluorenone,flavonoid,pituitary hormone,phagolysosomes,oligothiophene,fusogenic liposomes,hyaluronan

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