The continuity of abiotically formed bilayer membranes with similar structu
res in contemporary cellular life, and the requirement for microenvironment
s in which large and small molecules could be compartmentalized, support th
e idea that amphiphilic boundary structures contributed to the emergence of
life. As an extension of this notion, we propose here a 'Lipid World' scen
ario as an early evolutionary step in the emergence of cellular life on Ear
th. This concept combines the potential chemical activities of lipids and o
ther amphiphiles, with their capacity to undergo spontaneous self-organizat
ion into supramolecular structures such as micelles and bilayers. In partic
ular, the documented chemical rate enhancements within lipid assemblies sug
gest that energy-dependent synthetic reactions could lead to the growth and
increased abundance of certain amphiphilic assemblies. We further propose
that selective processes might act on such assemblies, as suggested by our
computer simulations of mutual catalysis among amphiphiles. As demonstrated
also by other researchers, such mutual catalysis within random molecular a
ssemblies could have led to a primordial homeostatic system displaying rudi
mentary life-like properties. Taken together, these concepts provide a theo
retical framework, and suggest experimental tests for a Lipid World model f
or the origin of life.