HYDROGEN-BONDING CONTROL OF MOLECULAR SELF-ASSEMBLY

In this short review we describe approaches to the design and construction of synthetic molecules that mimic the process of self organization that is at the heart of biological complexity. Multi-subunit enzymes, viruses, and higher order DNA structures ale formed by the non-covalent association of many smaller components. This self-assembly is controlled by the nature, number and orientation of interacting groups on the surface of the subunits. The central problem lies in overcoming the unfavorable entropy of multi-subunit association by significant enthalpic contribution from the binding of complementary regions on the subunits. We will place particular emphasis on the design of synthetic molecules that use hydrogen bonding interactions to control the formation of aggregates of well-defined structure.