“…For example, by intercalation of the amphiphilic molecules from the outer solution in the outer bilayer leaflet of the cell membrane (Sheetz and Singer, 1974;Svetina et al, 1982;Iglič and Hägerstrand, 1999), due to conformational changes of membrane proteins (Gimsa and Ried, 1995), or due to a lateral flow of membrane constituent molecules to the segment from the surrounding membrane (Israelachvili et al, 1976). The equilibrium A and shape of the segment at a given external condition are determined by the minimum of the total free energy of the system (Israelachvili et al, 1976;Wiese et al, 1992;Iglič et al, 1998) including the bending and relative stretching energy of the segment (Bukman et al, 1996), the shear energy (Evans and Skalak, 1980;Waugh, 1996;Iglič, 1997) and the energy due to inhomogeneous distributions of membrane components (Andelman et al, 1992;Lipowsky, 1993;Mohandas and Evans, 1994;Kralj-Iglič et al, 1996). However, it has been shown recently that the final shape of RBC microexovesicles is determined by the condition of the local extreme A (Iglič and Hägerstrand, 1999).…”