Cation-templated self-assembly of a lipophilic deoxyguanosine:: Solution structure of a K+-dG8 octamer

The lipophilic nucleoside 3',5'-didecanoyl-2'-deoxyguanosine, dG 1, extracts potassium salts from water into organic solvents. The K+ extraction drives the self-association of dG 1 to give G-quartet structures. A series of H-1 NMR experiments indicates that the identity of the assembled species in CDCl3 is modulated by the amount of K+ extracted by dG 1. At an 8:1 dG 1 to K+ picrate ratio, the octamer (dG 1)(8)-K+ predominates in solution, The (dG 1)(8)-K+ supramolecular complex, formed by coordination of a single K+ ion by eight dG 1 monomers, is robust and structurally unique. The H-1 NMR chemical shifts for both the exchangeable and nonexchangeable protons of(dG 1)(8)-K+ in CDCl3 were assigned from a combination of 2D H-1-H-1 and C-13-H-1 correlation experiments. One set of H-1 NMR signals corresponds to a dG 1 nucleoside with an anti conformation about the C(1')-N(9) glycosidic bond, whereas the other set of signals is due to 50% of the didecanoyl dG 1 adopting a syn conformation. Although the possible arrangements of an octamer containing a 1:1 ratio of anti dG 1 to syn dG 1 are many, the present NMR analysis leads to a defined single species composed of two G-quartets. In one tetramer, all of the dG 1 components have a syn conformation about the C(1')-N(9) glycosidic bond, while the other tetramer has an "all-anti" conformation. Moreover, intertetramer NOEs are consistent with stacking of the "all-anti" tetramer in a "head-to-tail" orientation on top of the "all-syn" tetramer, thus sandwiching a central K+ ion. This solution structure if;, to our knowledge; different from all of the assembled structures described so far for guanine aggregates. Presumably, the K+-bound octamer represents the first observable stage of the assembly process in the aggregation of dG 1.