Curvature stress modulation

A biologic reason for the abundance of nonlamellar lipids in membranes is that they possess the ability to modulate the activities of membrane proteins (15, 16). It has been recognized that membranes exist in a state of curvature frustration, which may be sufficiently large to have significant effect on certain protein conformations (17). Many examples show that the lipid bilayer elastic curvature stress indeed couples to conformational changes of membrane proteins (15, 18, 19). Protein kinase C is one such example of an enzyme activated by lipids that exhibit a propensity for nonlamellar phase formation (20). The activity of Ca " -ATPase from sarcoplasmic reticulum membranes also strongly correlates with the occurrence of nonbilayer lipids in the membrane and increases with the increase of their amount. It is noteworthy that the protein activity does not depend on the chemical structure of the lipids but only on their phase propensity thus specific binding interactions are ruled out. The list of proteins with activities that depend on the phase properties... 

The simple theory put forward by Meinhardt et al. accounts in a unified manner for both ripple phases and raft states in membranes. The prerequisites for the formation of such modulated phases is local phase separation (e.g., in the ripple case, between a liquid and a gel phase, or in the raft case, between a liquid disordered and a liquid ordered phase) and curvature stress in at least one of the two phases (typically the ordered one), resulting, e.g., from a size mismatch between head group and tails. In order to reproduce rippled states or rafts, coarsegrained simulation models must meet these criteria. This is often not the case. For example, the standard version of the popular MARTINI model does not have a ripple phase, because the low-temperature gel phase of saturated phospholipids is until ted. 

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