Literature DB >> 29851343

Highly Sensitive Lysine Deacetylase Assay Based on Acetylated Firefly Luciferase.

Martin Spinck1, Maria Ecke1, Sonja Sievers1, Heinz Neumann1.   

Abstract

Lysine deacetylases (KDACs) play important roles in many physiological processes and are implicated in many human diseases. Hence, the search for modulators of KDACs is very active, and reliable assays for monitoring their activity are key to success. Here, we describe a new KDAC assay based on Firefly luciferase harboring an acetylation on an essential active site lysine. We show that several KDACs can reverse this modification and hence activate luciferase. This new assay is extremely sensitive, reliable, and fast and can be performed in a continuous format. We used this assay to screen a small library of compounds and identified several novel effectors of SirT2 with low micromolar activity.

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Year:  2018        PMID: 29851343     DOI: 10.1021/acs.biochem.8b00483

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  2 in total

1.  14-3-3 Protein Bmh1 triggers short-range compaction of mitotic chromosomes by recruiting sirtuin deacetylase Hst2.

Authors:  Neha Jain; Petra Janning; Heinz Neumann
Journal:  J Biol Chem       Date:  2020-11-23       Impact factor: 5.157

2.  Evolved, Selective Erasers of Distinct Lysine Acylations.

Authors:  Martin Spinck; Petra Neumann-Staubitz; Maria Ecke; Raphael Gasper; Heinz Neumann
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-24       Impact factor: 15.336

  2 in total

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