Functional Motions of Candida antarctica Lipase B: A Survey through Open-Close Conformations

Candida antarctica lipase B (CALB) belongs to psychrophilic lipases which hydrolyze carboxyl ester bonds at low temperatures. There have been some features reported about cold-activity of the enzyme through experimental methods, whereas there is no detailed information on its mechanism of action at molecular level. Herein, a comparative molecular dynamics simulation and essential dynamics analysis have been carried out at three temperatures (5, 35 and 50 degrees C) to trace the dominant factors in the psychrophilic properties of CALB under cold condition. The results clearly describe the effect of temperature on CALB with meaningful differences in the flexibility of the lid region (alpha 5 helix), covering residues 141-147. Open-closed conformations have been obtained from different sets of long-term simulations (60 ns) at 5 degrees C gave two reproducible distinct forms of CALB. The starting open conformation became closed immediately at 35 and 50 degrees C during 60 ns of simulation, while a sequential open-closed form was observed at 5 degrees C. These structural alterations were resulted from alpha 5 helical movements, where the closed conformation of active site cleft was formed by displacement of both helix and its side chains. Analysis of normal mode showed concerted motions that are involved in the movement of both alpha 5 and alpha 10 helices. It is suggested that the functional motions needed for lypolytic activity of CALB is constructed from short-range movement of alpha 5, accompanied by long-range movement of the domains connected to the lid region.