Figure 9
From: Structure and mechanism of a redesigned multidrug transporter from the Major Facilitator Superfamily

Functional characterization of E26T/D34M/A150E. (a) Fluorescence measurement of a solution containing 2 µM E26T/D34M/A150E (red), revealing its ability to release one proton per protein molecule upon LDAO binding. As a comparison, the addition of LDAO to a solution containing 2 µM E26T/D34M (blue), failed to trigger the release of H+. (b) LDAO/H+ antiport observed in the everted membrane vesicles expressing E26T/D34M/A150E (red). H+ movement was monitored by measurement of acridine orange fluorescence, which is shown in arbitrary units (a.u.). By contrast, LDAO failed to induce H+ movement in the everted membrane vesicles harboring E26T/D34M (blue) or vector (black). The traces are representative of experiments performed in duplicate using two different preparations of everted membrane vesicles.