Spontaneous prebiotic formation of a β-ribofuranoside that self-assembles with a complementary heterocycle.

TitleSpontaneous prebiotic formation of a β-ribofuranoside that self-assembles with a complementary heterocycle.
Publication TypeJournal Article
Year of Publication2014
AuthorsChen, MC, Cafferty, BJ, Mamajanov, I, Gállego, I, Khanam, J, Krishnamurthy, R, Hud, NV
JournalJ Am Chem Soc
Volume136
Issue15
Pagination5640-6
Date Published2014 Apr 16
ISSN1520-5126
KeywordsCarbon-13 Magnetic Resonance Spectroscopy, Furans, Heterocyclic Compounds, Microscopy, Atomic Force, Prebiotics, Proton Magnetic Resonance Spectroscopy
Abstract

The RNA World hypothesis is central to many current theories regarding the origin and early evolution of life. However, the formation of RNA by plausible prebiotic reactions remains problematic. Formidable challenges include glycosidic bond formation between ribose and the canonical nucleobases, as well as the inability of nucleosides to mutually select their pairing partners from a complex mixture of other molecules prior to polymerization. Here we report a one-pot model prebiotic reaction between a pyrimidine nucleobase (2,4,6-triaminopyrimidine, TAP) and ribose, which produces TAP-ribose conjugates in high yield (60-90%). When cyanuric acid (CA), a plausible ancestral nucleobase, is mixed with a crude TAP+ribose reaction mixture, micrometer-length supramolecular, noncovalent assemblies are formed. A major product of the TAP+ribose reaction is a β-ribofuranoside of TAP, which we term TARC. This nucleoside is also shown to efficiently form supramolecular assemblies in water by pairing and stacking with CA. These results provide a proof-of-concept system demonstrating that several challenges associated with the prebiotic emergence of RNA, or pre-RNA polymers, may not be as problematic as widely believed.

DOI10.1021/ja410124v
Alternate JournalJ. Am. Chem. Soc.
PubMed ID24328232