Abstract

Recently, two members of the P4 family of P-type ATPases, Dnf1p and Dnf2p, were shown to be necessary for the internalization (flip) of fluorescent, 7-nitrobenz-2-oxa-1,3-diazol-4-yl(NBD)-labeled phospholipids across the plasma membrane of Saccharomyces cerevisiae. In the current study, we have demonstrated that ATP hydrolysis is not sufficient for phospholipid flip in the absence of the proton electrochemical gradient across the plasma membrane. This requirement was demonstrated by two independent means. First, collapse of the plasma membrane proton electrochemical gradient by the protonophore, carbonyl cyanide m-chlorophenylhydrazone (CCCP) almost completely blocked NBD-phospholipid flip while only moderately reducing the cytosolic ATP concentration. Second, strains with point mutations in PMA1, which encodes the plasma membrane proton pump that generates the proton electrochemical gradient, are defective in NBD-PC flip, whereas their cytosolic ATP content is actually increased. These results establish that the proton electrochemical gradient is required for NBD-phospholipid flip across the plasma membrane of yeast and raise the question whether it contributes an additional required driving force or whether it functions as a regulatory signal.

Highlights

  • In Saccharomyces cerevisiae, it was recently shown that deletion of two members of the P4 subfamily, DNF1 and DNF2, results in a significant decrease in the flip of NBD2-labeled phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine (NBD-PC, NBD-PE, and NBD-PS) [8]

  • Inhibition of NBD-PC Flip by carbonyl cyanide m-chlorophenylhydrazone (CCCP) Is Not Correlated with a Reduction in Cellular ATP—In previous work from our laboratory, we have demonstrated that collapse of the proton electrochemical gradient across the plasma membrane almost completely blocks the flip of NBD-PC and NBD-PE [11] under conditions that were not expected to significantly lower cytosolic ATP levels [13]

  • To confirm and extend this observation, we have measured the internalization of NBD-PC on ice and the cellular ATP levels following the treatment of yeast with varying concentrations of CCCP (Fig. 1)

Read more

Summary

Introduction

In Saccharomyces cerevisiae, it was recently shown that deletion of two members of the P4 subfamily, DNF1 and DNF2, results in a significant decrease in the flip of NBD2-labeled phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine (NBD-PC, NBD-PE, and NBD-PS) [8]. These data were interpreted to indicate that the plasma membrane proton electrochemical gradient is necessary for the flip of NBD-labeled phospholipids, even in the presence of normal levels of cytosolic ATP [11].

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call