Studies on Pyry I retinal Analogues of Bacteriorhodopsin

Abstract

AbstractThe retinal analogues 3‐methyl‐5‐(l‐pyryl)‐2E,4E‐penta‐dienal (1) and 3,7‐dimethyl‐9‐(l‐pyryl)‐2E,4E,6E,8E‐non‐atetraenal (2), which contain the tetra aromatic pyryl system, have been synthesized and characterized in order to examine the effect of the extended ring system on the binding capabilities and the function of bacteriorhodopsin (bR). The two bR mutants, E194Q and E204Q, known to have distinct proton‐pumping patterns, were also examined so that the effect of the bulky ring system on the proton‐pumping mechanism could be studied. Both retin‐als formed pigments with all three bacterioopsins, and these pigments were found to have absorption maxima in the range 498–516 nm. All the analogue pigments showed activity as proton pumps. The pigment formed from wild‐type apoprotein bR with 1 (with the shortened polyene side chain) showed an M intermediate at 400 nm and exhibited fast proton release followed by proton uptake. Extending the polyene side chain to the length identical with retinal, analogue 2 with wild‐type apoprotein gave a pigment that shows M and O intermediates at 435 nm and 650 nm, respectively. This pigment shows both fast and slow proton release at pH 7, suggesting that the pKa of the proton release group (in the M‐state) is higher in this pigment compared to native bR. Hydrogen azide ions were found to accelerate the rise and decay of the O intermediate at neutral pH in pyryl 2 pigment. The pigments formed between 2 and E194Q and E204Q showed proton‐pumping behavior similar to pigments formed with the native retinal, suggesting that the size of the chromophore ring does not alter the protein conformation at these sites.