Literature DB >> 22026187

Searching for the protein targets of bioactive molecules.

Christopher Chidley1, Hirohito Haruki, Miriam Grønlund Pedersen, Cindy Fellay, Simone Moser, Kai Johnsson.   

Abstract

The identification of all protein targets of a given drug or bioactive molecule within the human body is a prerequisite for an understanding of its beneficial and deleterious activities. Current approaches to reveal protein targets often fail to reveal physiologically relevant interactions. Here we review a recently introduced yeast-based approach for the identification of the binding partners of small molecules. We discuss the advantages and limitations of the approach using the clinically approved drug sulfasalazine as an example.

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Year:  2011        PMID: 22026187     DOI: 10.2533/chimia.2011.720

Source DB:  PubMed          Journal:  Chimia (Aarau)        ISSN: 0009-4293            Impact factor:   1.509


  3 in total

1.  The why and how of phenotypic small-molecule screens.

Authors:  Ulrike S Eggert
Journal:  Nat Chem Biol       Date:  2013-04       Impact factor: 15.040

2.  Imaging of RNAs in live cells with spectrally diverse small molecule fluorophores.

Authors:  Tucker J Carrocci; Aaron A Hoskins
Journal:  Analyst       Date:  2013-11-01       Impact factor: 4.616

3.  Target Abundance-Based Fitness Screening (TAFiS) Facilitates Rapid Identification of Target-Specific and Physiologically Active Chemical Probes.

Authors:  Arielle Butts; Christian DeJarnette; Tracy L Peters; Josie E Parker; Morgan E Kerns; Karen E Eberle; Steve L Kelly; Glen E Palmer
Journal:  mSphere       Date:  2017-10-04       Impact factor: 4.389

  3 in total

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