Literature DB >> 20162536

Reagents for investigating MAPK signalling in model yeast species.

David Pincus1, Kirsten Benjamin, Ian Burbulis, Annie E Tsong, Orna Resnekov.   

Abstract

Here we present a set of resources (bacterial expression plasmids and antibodies) for the interrogation of proteins involved in yeast MAPK signalling. We constructed bacterial protein expression plasmids for 25 proteins involved in MAPK signalling in budding yeast. From these constructs we expressed and purified proteins and generated rabbit polyclonal antibodies against 13 proteins in the pheromone MAPK pathway. We verified the specificity of the antibodies and employed them to follow pathway proteins in cells stimulated with pheromone. We show that these reagents can be used to detect pheromone-induced post-translational modifications and changes in the oligomeric state of pathway proteins. In addition to recognizing their target proteins in Saccharomyces cerevisiae, these antibodies allow the detection of predicted orthologues in the distant evolutionary relatives Kluyveromyces lactis and Schizosaccharomyces pombe. These antibodies are new tools for investigating MAPK signalling in model yeast species and may be useful for studying MAPK signalling in higher eukaryotes.

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Year:  2010        PMID: 20162536     DOI: 10.1002/yea.1758

Source DB:  PubMed          Journal:  Yeast        ISSN: 0749-503X            Impact factor:   3.239


  4 in total

1.  Engineering allosteric regulation in protein kinases.

Authors:  David Pincus; Jai P Pandey; Zoë A Feder; Pau Creixell; Orna Resnekov; Kimberly A Reynolds
Journal:  Sci Signal       Date:  2018-11-06       Impact factor: 8.192

2.  Scaffold number in yeast signaling system sets tradeoff between system output and dynamic range.

Authors:  Ty M Thomson; Kirsten R Benjamin; Alan Bush; Tonya Love; David Pincus; Orna Resnekov; Richard C Yu; Andrew Gordon; Alejandro Colman-Lerner; Drew Endy; Roger Brent
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-23       Impact factor: 11.205

3.  Variable Dependence of Signaling Output on Agonist Occupancy of Ste2p, a G Protein-coupled Receptor in Yeast.

Authors:  Rajashri Sridharan; Sara M Connelly; Fred Naider; Mark E Dumont
Journal:  J Biol Chem       Date:  2016-09-19       Impact factor: 5.157

4.  Assigning quantitative function to post-translational modifications reveals multiple sites of phosphorylation that tune yeast pheromone signaling output.

Authors:  David Pincus; Christopher J Ryan; Richard D Smith; Roger Brent; Orna Resnekov
Journal:  PLoS One       Date:  2013-03-12       Impact factor: 3.240

  4 in total

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