The pST44 polycistronic expression system for producing protein complexes in Escherichia coli

• Published in: Protein expression and purification 2005-04, Vol.40 (2), p.385-395
• Main Authors: Tan, Song, Kern, Ronald C., Selleck, William
• Format: Article
• Language: English
• Subjects: Acetyltransferases - genetics; Affinity Labels; Affinity tags; Cloning, Molecular - methods; Coexpression of protein complexes; Fungal Proteins; Genes; Histone acetyltransferase; Histone Acetyltransferases; Humans; Molecular Probes; Multiprotein Complexes - genetics; Mutation; Plasmids; Polycistronic expression; Protein Subunits - genetics; Recombinant expression; Recombinant Proteins - genetics
• ISSN: 1046-5928; 1096-0279
• DOI: 10.1016/j.pep.2004.12.002

Protein complexes are responsible for key biological processes, but methods to produce recombinant protein complexes for biochemical and biophysical studies are limited. We have developed a second generation Escherichia coli polycistronic expression system which improves on the modularity of our original pST39 polycistronic system. This pST44 expression system simplifies the construction of polycis-tronic plasmids, particularly of variant plasmids expressing deletion or point mutations in any subunit. To facilitate purification of the expressed complex, we have prepared a suite of 72 plasmids which allows individual subunits to be tagged at the N- or C-terminus with six permanent or cleavable peptide affinity tags. We demonstrate these new features in a detailed deletion analysis of a three protein yeast Piccolo NuA4 histone acetyltransferase complex, and in the affinity purification of a human Piccolo NuA4 complex. We also utilize the modular design to show that the order of expression of the three subunits along the polycistronic plasmid does not affect the reconstitution of the yeast Piccolo complex in E. coli.