Analysis of Ethylene Receptors: Assay for Histidine Kinase Activity

The ethylene receptors of plants exist in two subfamilies. Members of subfamily-1 have functional histidine kinase domains, whereas members of subfamily-2 have diverged histidine-kinase-like domains that in some cases have been shown to exhibit Ser/Thr kinase activity. Here, we describe a method to biochemically characterize the enzymatic activity of these kinase domains in vitro. For this purpose, the histidine kinase domain of the receptors is transgenically expressed in yeast as a fusion to glutathione-S-transferase (GST) for subsequent affinity purification. Autophosphorylation activity is assessed by the use of an in vitro kinase assay with the purified protein. Acid/base stability of the incorporated phosphate can then be used as a diagnostic for whether His, Asp, or Ser/Thr/Tyr is phosphorylated.