Ratiometric Measurement of Protein Abundance after Transient Expression of a Transgene in .

Ratiometric reporters are tools to dynamically measure the relative abundance of a protein of interest. In these systems, a target protein fused to a fluorescent or bioluminescent reporter is expressed with fixed stoichiometry to a reference protein fused to a second reporter. Both fusion proteins are encoded on a single transcript but are separated during translation by a 2A "self-cleaving" peptide. This approach enables changes in the relative abundance of a target protein to be detected sensitively, reducing variability in expression of the ratiometric reporter transgene that may occur across different tissues or transformation events. We recently developed a set of Gateway-compatible plant transformation vectors termed pRATIO that combine a variety of promoters, fluorescent and bioluminescent reporters, and 2A peptides derived from foot-and-mouth disease virus. Here, we describe in detail how to use the dual-fluorescent ratiometric reporter pRATIO3212 to examine the relative abundance of a target protein after transient expression in leaves. For this example, we analyze degradation of the SUPPRESSOR OF MAX2 1 (SMAX1) protein from in response to treatments with karrikins and -GR24. This protocol provides a simple, rapid, and readily scalable method for analysis of relative protein abundance in -infiltrated leaf tissues.