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      Identification of a chemical probe for NAADP by virtual screening

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          Abstract

          Research into the biological role of the Ca 2+-releasing second messenger NAADP (nicotinic acid adenine dinucleotide phosphate) has been hampered by a lack of chemical probes. To find new chemical probes for exploring NAADP signaling, we turned to virtual screening, which can evaluate millions of molecules rapidly and inexpensively. We used NAADP as the query ligand to screen the chemical library ZINC for compounds with 3D-shape and electrostatic similarity. We tested the top-ranking hits in a sea urchin egg bioassay and found that one hit, Ned-19, blocks NAADP signaling at nanomolar concentrations. In intact cells, Ned-19 blocked NAADP signaling and fluorescently labeled NAADP receptors. Moreover, we show the utility of Ned-19 as a chemical probe by using it to demonstrate that NAADP is a key causal link between glucose sensing and Ca 2+ increases in mouse pancreatic beta cells.

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          Most cited references46

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          The fluorescent toolbox for assessing protein location and function.

          Advances in molecular biology, organic chemistry, and materials science have recently created several new classes of fluorescent probes for imaging in cell biology. Here we review the characteristic benefits and limitations of fluorescent probes to study proteins. The focus is on protein detection in live versus fixed cells: determination of protein expression, localization, activity state, and the possibility for combination of fluorescent light microscopy with electron microscopy. Small organic fluorescent dyes, nanocrystals ("quantum dots"), autofluorescent proteins, small genetic encoded tags that can be complexed with fluorochromes, and combinations of these probes are highlighted.
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            Virtual screening of chemical libraries.

            Virtual screening uses computer-based methods to discover new ligands on the basis of biological structures. Although widely heralded in the 1970s and 1980s, the technique has since struggled to meet its initial promise, and drug discovery remains dominated by empirical screening. Recent successes in predicting new ligands and their receptor-bound structures, and better rates of ligand discovery compared to empirical screening, have re-ignited interest in virtual screening, which is now widely used in drug discovery, albeit on a more limited scale than empirical screening.
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              The many roles of computation in drug discovery.

              An overview is given on the diverse uses of computational chemistry in drug discovery. Particular emphasis is placed on virtual screening, de novo design, evaluation of drug-likeness, and advanced methods for determining protein-ligand binding.
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                Author and article information

                Journal
                101231976
                32624
                Nat Chem Biol
                Nat. Chem. Biol.
                Nature chemical biology
                1552-4450
                1552-4469
                4 February 2009
                22 February 2009
                April 2009
                01 October 2009
                : 5
                : 4
                : 220-226
                Affiliations
                [1 ]University of Oxford, Department of Pharmacology, Mansfield Road, Oxford OX1 3QT, United Kingdom.
                [2 ]University of Southampton, Department of Chemistry, Highfield, Southampton, SO17 1BJ, United Kingdom.
                [3 ]Okayama University, Graduate School of Natural Science and Technology, 1-1-1 Tsushimanaka, Okayama 700-8530, Japan
                Author notes
                [4]

                These authors contributed equally.

                [5 ] Correspondence: Grant C. Churchill, Email: grant.churchill@ 123456pharm.ox.ac.uk
                Article
                UKMS3828
                10.1038/nchembio.150
                2659327
                19234453
                efd22359-fa18-4473-8c3d-e6666db90716
                History
                Funding
                Funded by: Biotechnology and Biological Sciences Research Council :
                Award ID: BB/D012694/1 || BB_
                Categories
                Article

                Biochemistry
                Biochemistry

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