Literature DB >> 17264931

Supramolecular architectures generated by self-assembly of guanosine derivatives.

Jeffery T Davis1, Gian Piero Spada.   

Abstract

Nature's use of a simple genetic code to enable life's complex functions is an inspiration for supramolecular chemistry. DNA nucleobases carry the key information utilizing a variety of cooperative and non-covalent interactions such as hydrophobic, van der Waals, pi-pi stacking, ion-dipole and hydrogen bonding. This tutorial review describes some recent advances in the form and function provided by self-assembly of guanine (G) based systems. We attempt to make connections between the structures of the assemblies and their properties. The review begins with a brief historical context of G self-assembly in water and then describes studies on lipophilic guanosine analogs in organic solvents. The article also focuses on examples of how G analogs have been used as building blocks for functional applications in supramolecular chemistry, material science and nanotechnology.

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Year:  2006        PMID: 17264931     DOI: 10.1039/b600282j

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  74 in total

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Review 7.  High-definition self-assemblies driven by the hydrophobic effect: synthesis and properties of a supramolecular nanocapsule.

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9.  Tuning thermoresponsive supramolecular G-quadruplexes.

Authors:  José E Betancourt; José M Rivera
Journal:  Langmuir       Date:  2015-02-10       Impact factor: 3.882

10.  Encapsulating a single G-quadruplex aptamer in a protein nanocavity.

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