Insight into the Cation-π Interaction at the Metal Binding Site of the Copper Metallochaperone CusF.

The periplasmic Cu+/Ag+ chaperone CusF features a novel cation-π interaction between a Cu+/Ag+ ion and Trp44 at the metal binding site. The nature and strength of the Cu+/Ag+-Trp44 interactions were investi- gated using computational methodologies. Quantum-mechanical (QM) calculations showed that the Cu+ and Ag+ interactions with Trp44 are of similar strength (∼14 kcal/ mol) and bond order. Quantum-mechanical/molecular-mechanical (QM/MM) calculations showed that Cu binds in a distorted tetrahedral coordination environment in the Trp44Met mutant, which lacks the cation-π interaction. Molecular dynamics (MD) simulations of CusF in the apo and Cu+-bound states emphasized the importance of the Cu+-Trp44 interaction in protecting Cu from water oxidation. The protein structure does not change over the time scale of hundreds of nanoseconds in the metal-bound state. The metal recognition site exhibits small motions in the apo state but remains largely preorganized toward metal binding. Trp44 remains oriented to form the cation-π interaction in the apo state and faces an energetic penalty to move away from the metal ion. Cu+ binding quenches the protein's internal motions in regions linked to binding CusB, suggesting that protein motions play an essential role in Cu+ transfer to CusB. [ABSTRACT FROM AUTHOR]