Abstract
Cyclic nucleotides such as 3′,5′-cyclic adenosine monophosphate (cAMP) and 3′,5′-cyclic guanosine monophosphate (cGMP) are increasingly recognized as key signaling molecules in plants, and a growing number of plant mononucleotide cyclases, both adenylate cyclases (ACs) and guanylate cyclases (GCs), have been reported. Catalytically active cytosolic GC domains have been shown to be part of many plant receptor kinases and hence directly linked to plant signaling and downstream cellular responses. Here we detail, firstly, methods to identify and express essential functional GC domains of receptor kinases, and secondly, we describe mass spectrometric methods to quantify cGMP generated by recombinant GCs from receptor kinases in vitro.
Original language | English (US) |
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Title of host publication | Methods in Molecular Biology |
Publisher | Humana Press Inc. |
Pages | 131-140 |
Number of pages | 10 |
DOIs | |
State | Published - 2017 |
Publication series
Name | Methods in Molecular Biology |
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Volume | 1621 |
ISSN (Print) | 1064-3745 |
Bibliographical note
Publisher Copyright:© 2017, Springer Science+Business Media LLC.
Keywords
- Cyclic nucleotides
- Guanylate cyclase
- HPLC
- Nucleotide cyclase
- Tandem mass spectrometry
- cGMP
ASJC Scopus subject areas
- Genetics
- Molecular Biology