Expression of Reticulomyxa filosa alpha- and beta-tubulins in Escherichia coli yields soluble and partially correctly folded material.

Tubulins are highly conserved multidomain proteins that have to interact with eukaryotic chaperonins to gain their correct three-dimensional conformation. The prokaryotic chaperonin system of GroEL/ES is able to generate intermediate folding states but not natively folded tubulin. To create a system for studying these folding intermediates, tubulins from the giant amoeba Reticulomyxa filosa (alpha 2- and beta 2-tubulin) were expressed in Escherichia coli singly or in tandem. In all cases, soluble tubulin was generated in amounts of 5-10 mg/l culture. This is the first reported expression of soluble tubulin in bacterial cells. Of particular interest was the observation that upon coexpression with R. filosa beta 2-tubulin, proteolytic degradation of alpha 2-tubulin was reduced and more full-length product remained intact. This observation points to a specific interaction of alpha 2- and beta 2-tubulins in the E. coli cell. The sites of interaction are most probably the same that are responsible for the binding of native alpha 2- and beta 2-tubulin. The established expression system therefore seems well suited for further studies concerning the folding of tubulins.