1. Mechanism of Proton Transfer Inhibition by Cd2+ Binding to Bacterial Reaction Centers: Determination of the pKA of Functionally Important Histidine Residues
- Author
-
Melvin Y. Okamura, Tehrani A, George Feher, Beatty Jt, Laura B. Sagle, and Mark L. Paddock
- Subjects
Models, Molecular ,Photosynthetic reaction centre ,Proton ,Stereochemistry ,Photosynthetic Reaction Center Complex Proteins ,Mutant ,Rhodobacter sphaeroides ,Biochemistry ,Electron Transport ,chemistry.chemical_compound ,Electron transfer ,Imidazole ,Histidine ,Aspartic Acid ,Binding Sites ,biology ,Quinones ,Hydrogen-Ion Concentration ,biology.organism_classification ,Recombinant Proteins ,Quinone ,Kinetics ,chemistry ,Mutagenesis, Site-Directed ,Protons ,Cadmium ,Protein Binding - Abstract
The bacterial photosynthetic reaction center (RC) uses light energy to catalyze the reduction of a bound quinone molecule Q(B) to quinol Q(B)H(2). In RCs from Rhodobacter sphaeroides the protons involved in this process come from the cytoplasm and travel through pathways that involve His-H126 and His-H128 located near the proton entry point. In this study, we measured the pH dependence from 4.5 to 8.5 of the binding of the proton transfer inhibitor Cd(2+), which ligates to these surface His in the RC and inhibits proton-coupled electron transfer. At pH6, the negative slope of the logarithm of the dissociation constant, K(D), versus pH approaches 2, indicating that, upon binding of Cd(2+), two protons are displaced; i.e., the binding is electrostatically compensated. At pH7, K(D) becomes essentially independent of pH. A theoretical fit to the data over the entire pH range required two protons with pK(A) values of 6.8 and 6.3 (+/-0.5). To assess the contribution of His-H126 and His-H128 to the observed pH dependence, K(D) was measured in mutant RCs that lack the imidazole group of His-H126 or His-H128 (His --Ala). In both mutant RCs, K(D) was approximately pH independent, showing that Cd(2+) does not displace protons upon binding in the mutant RCs, in contrast to the native RC in which His-H126 and His-H128 are the predominant contributors to the observed pH dependence of K(D). Thus, Cd(2+) inhibits RC function by binding to functionally important histidines.
- Published
- 2003