The rate-determining step in cAMP-mediated exocytosis in the rat parotid and submandibular glands appears to involve analogous 26-kDa integral membrane phosphoproteins.

The possible direct involvement of protein phosphorylation in the regulation of exocytosis during beta-adrenergic receptor stimulation in rat parotid and submandibular salivary glands was investigated in vitro using dispersed cells. The dispersed cells were labeled with [32P]orthophosphate for 40 min prior to experimental manipulation. Subcellular fractions were isolated, the proteins were separated using sodium dodecylsulfate/polyacrylamide gel electrophoresis (NaDodSO4/PAGE), and the phosphoproteins were detected by autoradiography. Changes in the extent of phosphorylation for each phosphoprotein were determined indirectly by densitometric analyses. The analogous parotid and submandibular 26-kDa membrane phosphoproteins had a rapid phosphate turnover rate (t 1/2 = 5-6 min) whereas the analogous 21-kDa membrane phosphoproteins had a much slower phosphate turnover rate (t 1/2 greater than 20 min). The results of Triton X-114 extraction indicated that the 26- and 21-kDa phosphoproteins were integral membrane proteins. The rate of phosphate turnover for the analogous 26-kDa phosphoproteins is compatible with a regulatory role in exocytosis, whereas the slower phosphate turnover rate for the analogous 21-kDa phosphoproteins suggests that these proteins may play a more subordinate role in secretion or they may coordinate secretion with other cellular metabolic events.