Literature DB >> 22500607

Supramolecular displacement-mediated activation of a silent fluorescence probe for label-free ligand screening.

Diego Amado Torres1, Malar A Azagarsamy, S Thayumanavan.   

Abstract

We report a new approach for the rapid screening of analyte binding affinities for a target protein. We demonstrate that a molecular probe, with a pro-fluorophore substrate and ligand moieties, can be hindered from enzymatic access when bound to the target protein. When analytes displace the probe from the protein's binding pocket, a fluorescence profile is generated. This profile is used to discriminate analytes based on their relative binding affinities.
© 2012 American Chemical Society

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Year:  2012        PMID: 22500607      PMCID: PMC3342419          DOI: 10.1021/ja301204z

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  20 in total

Review 1.  High-throughput X-ray crystallography for drug discovery.

Authors:  Tom L Blundell; S Patel
Journal:  Curr Opin Pharmacol       Date:  2004-10       Impact factor: 5.547

Review 2.  Applications of ESI-MS in drug discovery: interrogation of noncovalent complexes.

Authors:  Steven A Hofstadler; Kristin A Sannes-Lowery
Journal:  Nat Rev Drug Discov       Date:  2006-07       Impact factor: 84.694

3.  Thermodynamic stability of carbonic anhydrase: measurements of binding affinity and stoichiometry using ThermoFluor.

Authors:  Daumantas Matulis; James K Kranz; F Raymond Salemme; Matthew J Todd
Journal:  Biochemistry       Date:  2005-04-05       Impact factor: 3.162

4.  Structural analysis of charge discrimination in the binding of inhibitors to human carbonic anhydrases I and II.

Authors:  D K Srivastava; Kevin M Jude; Abir L Banerjee; Manas Haldar; Sumathra Manokaran; Joel Kooren; Sanku Mallik; David W Christianson
Journal:  J Am Chem Soc       Date:  2007-04-04       Impact factor: 15.419

Review 5.  Affinity selection-mass spectrometry screening techniques for small molecule drug discovery.

Authors:  D Allen Annis; Elliot Nickbarg; Xianshu Yang; Michael R Ziebell; Charles E Whitehurst
Journal:  Curr Opin Chem Biol       Date:  2007-10-10       Impact factor: 8.822

6.  The future of high-throughput screening.

Authors:  Lorenz M Mayr; Peter Fuerst
Journal:  J Biomol Screen       Date:  2008-07

Review 7.  Calorimetry and thermodynamics in drug design.

Authors:  Jonathan B Chaires
Journal:  Annu Rev Biophys       Date:  2008       Impact factor: 12.981

Review 8.  Investigation of protein-ligand interactions by mass spectrometry.

Authors:  Andrea Sinz
Journal:  ChemMedChem       Date:  2007-04       Impact factor: 3.466

9.  Carbonic anhydrase inhibitors, interaction of boron derivatives with isozymes I and II: a new binding site for hydrophobic inhibitors at the entrance of the active site as shown by docking studies.

Authors:  C Chazalette; M Riviere-Baudet; A Scozzafava; F Abbate; Z Ben Maarouf; C T Supuran
Journal:  J Enzyme Inhib       Date:  2001

10.  Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors.

Authors:  Daniel A Bachovchin; Justin T Mohr; Anna E Speers; Chu Wang; Jacob M Berlin; Timothy P Spicer; Virneliz Fernandez-Vega; Peter Chase; Peter S Hodder; Stephan C Schürer; Daniel K Nomura; Hugh Rosen; Gregory C Fu; Benjamin F Cravatt
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-11       Impact factor: 11.205

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