Raji Misjudeen, Gehring Chris
Analytical Core Laboratory, 4700 King Abdullah University of Science and Technology, Thuwal, 23955-6900, Kingdom of Saudi Arabia.
Division of Biological & Environmental Science & Engineering, 4700 King Abdullah University of Science and Technology, Thuwal, 23955-6900, Kingdom of Saudi Arabia.
Methods Mol Biol. 2017;1621:131-140. doi: 10.1007/978-1-4939-7063-6_13.
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.
诸如3',5'-环磷酸腺苷(cAMP)和3',5'-环磷酸鸟苷(cGMP)等环核苷酸越来越被认为是植物中的关键信号分子,并且已经报道了越来越多的植物单核苷酸环化酶,包括腺苷酸环化酶(ACs)和鸟苷酸环化酶(GCs)。具有催化活性的胞质GC结构域已被证明是许多植物受体激酶的一部分,因此与植物信号传导和下游细胞反应直接相关。在这里,我们首先详细介绍鉴定和表达受体激酶必需功能GC结构域的方法,其次,我们描述了通过质谱法对重组GCs在体外由受体激酶产生的cGMP进行定量的方法。