Reconstitution of the heliobacterial photochemical reaction center and cytochrome c553 into a proteoliposome system

The heliobacterial reaction center (HbRC) is the simplest known photochemical reaction center, in terms of its polypeptide composition. In the heliobacterial cells, its electron donor is a cytochrome (cyt) c(553) attached to the membrane via a covalent linkage with a diacylglycerol. We have reconstituted purified HbRC into liposomes mimicking the phospholipid composition of heliobacterial membranes. We also incorporated a lipid with a headgroup containing Ni(II):nitrilotriacetate (NTA) to provide a binding site for the soluble version of the heliobacterial cyt c(553) in which the N-terminal membrane attachment site is replaced by a hexahistidine tag. The HbRC was inserted into the liposomes with the donor side preferentially exposed to the exterior; this bias increased to nearly 100% with higher concentrations (>= 10 mol%) of the Ni(II)-NTA lipid in the membrane, and is most likely due to the net negative charge of the surface of the membrane. The HbRC in proteoliposomes without the Ni(II)-NTA lipid exhibited normal charge separation and subsequent charge recombination of the P800 +FX- state in 15 ms; however, the oxidized primary donor (P800+) was not significantly reduced by added H-6-cyt c(553). In contrast, with proteoliposomes containing the Ni(II)-NTA lipid, addition of H-6-cyt c(553) resulted in a new kinetic component resulting from fast reduction (2-5 ms) of P800+ by H-6-cyt c(553). The contribution of this kinetic component varied with the concentration of added H-6-cyt c(553) and could represent 80% or more of the total P800+ decay. Thus, the HbRC and its interaction with its native electron donor have been reconstituted into an artificial membrane system.