Guest Editor: R. Haag
Beilstein J. Org. Chem. 2015, 11, 848–849. https://doi.org/10.3762/bjoc.11.94
Received 06 May 2015, Accepted 07 May 2015, Published 19 May 2015
Keywords: glycoarchitectures; supramolecular chemistry; multivalency; multivalent protein inhibitors; pathogen binding
Multivalency is a key principle in nature to establish strong, but also reversible chemical interactions between two units, e.g., a receptor and a ligand, viruses and host cells, or between two cell surfaces. Multivalent binding is based on multiple simultaneous molecular recognition processes and plays an important role in the self-organization of matter, in biological recognition processes as well as in signal transduction in biological systems. The targeted development of multivalent molecules is not only used for the strong inhibition of proteins and prevention of pathogen infections, but also allows for the selective production of functional molecular architectures and surface structures as well as the controlled interaction of multivalent surfaces. The chemical and biological mechanisms and the influence of scaffold architectures with different dimensions for multivalent interactions have not been comprehensively explored. Thus, the experimental and theoretical understanding of defined oligovalent binding systems requires further detailed understanding in the gas phase, in solution and on surfaces.
Frequently the interaction of a single ligand with an acceptor (monovalent interaction) in many cases can be quantitatively understood. This, however, is completely different, when several covalently linked ligands of the same or of a similar nature bind to an ensemble of acceptors (multivalent interactions) . Due to the multiple additive (in some cases cooperative) interactions the equilibrium will shift and bond reinforcement occurs (Figure 1). Also, the kinetically controlled dissociation can become very slow to almost non-existent. Multivalency is also dependent on the size, shape and flexibility of the scaffold architecture, especially for the interfacial interaction with biological systems.
In order to obtain a deeper understanding of multivalent interactions this Thematic Series in the Beilstein Journal of Organic Chemistry puts its focus to unravel new cellular interactions that are highly relevant  and systematically combines theoretical exploration of defined multivalent supramolecular interactions  as well as new supramolecular designer systems [4,5]. The influence of spacer length and flexibility on the binding affinity of ligands  will be examined as well as the mechanical stability of complexes . Furthermore, the Thematic Series covers the synthesis of various new glycoarchitectures for multivalent interactions [8-12] and studies the scope of multivalent lectin-glycointeractions in galectins , with iminosugars  and carbohydrate mimetics . This Thematic Series in the Beilstein Journal of Organic Chemistry also investigates the enhanced multivalent binding of protein scaffolds , peptide–polymer interactions [17-20] tripodal-catecholates  and polycatechol–surface interactions  as well as multivalent organocatalyts . Finally, multivalent dendritic poly(arginine/histidine)-siRNA complexes are evaluated regarding their transfection efficiency .
In the future a deeper understanding of multivalent interactions at all length scales from the nanometer to the micrometer range is crucial for solving important problems and for the development of new systems in the fields of life and materials science. In order to address this highly complex and long-term challenge, the interdisciplinary cooperation of scientists with different expertise ranging from biochemistry to theory is essential.
Berlin, May 2015