Previous studies on the mechanism of enteropathogenicEscherichia coli (EPEC) infection have revealed an increase in the phosphorylation state of a number of proteins in human laryngeal HEp‐2 cells. The most prominent was an acidic phosphoprotein(s) ofM r 20–21 kDa. The present study reports: (a) a simple method for purification of phosphorylated 20 kDa protein: (b) identification of the 20 kDa phosphoprotein as myosin light chain; and (c) that the phorbol ester. TPA, also increased the phosphorylation of the 20 kDa myosin light chain. In contrast to the effects of EPEC, TPA stimulation resulted in the dissociation of myosin from the cytoskeleton to the cytosol.
