X-RAY CRYSTAL-STRUCTURE AND MOLECULAR-DYNAMICS SIMULATION OF BOVINE PANCREAS PHOSPHOLIPASE A(2)-N-DODECYLPHOSPHORYLCHOLINE COMPLEX

The crystal structure of n-dodecylphosphorylcholine (n-C12PC)-bovine pancreas phospholipase A(2) (PLA(2)) complex provided the following structural characteristics: (1) the dodecyl chain of n-C12PC was located at the PLA(2) N-terminal helical region by hydrophobic interactions, which corresponds to the binding pocket of 2-acyl fatty acid chain (beta-chain) of the substrate phospholipid, (2) the region from Lys-53 to Lys-56 creates a choline-receiving pocket of n-C12PC and (3) the N-terminal group of Ala-1 shifts significantly toward the Tyr-52 OH group by the binding of the n-C12PC inhibitor. Since the accuracy of the X-ray analysis (R = 0.275 at 2.3 Angstrom resolution) was insufficient to establish these important X-ray insights, the complex structure was further investigated through the molecular dynamics (MD) simulation, assuming a system in aqueous solution at 310K. The MD simulation covering 176 ps showed that the structural characteristics observed by X-ray analysis are intrinsic and also stable in the dynamic state. Furthermore, the MD simulation made clear that the PLA(2) binding pocket is large enough to permit the conformational fluctuation of the n-C12PC hydrocarbon chain. (C) 1994 Wiley-Liss, Inc.