Issue 91, 2015

Synthesis and base pairing studies of geranylated 2-thiothymidine, a natural variant of thymidine

Abstract

The synthesis and base pairing of DNA duplexes containing the geranylated 2-thiothymidine have been investigated. This naturally existing hydrophobic modification could grant better base pairing stability to the T–G pair over normal T–A and other mismatched pairs in the duplex context. This study provides a potential explanation for the different codon recognition preferences of the geranylated tRNAs.

Graphical abstract: Synthesis and base pairing studies of geranylated 2-thiothymidine, a natural variant of thymidine

Supplementary files

Article information

Article type
Communication
Submitted
06 Sep 2015
Accepted
15 Sep 2015
First published
15 Sep 2015

Chem. Commun., 2015,51, 16369-16372

Author version available

Synthesis and base pairing studies of geranylated 2-thiothymidine, a natural variant of thymidine

R. Wang, S. V. Ranganathan, M. Basanta-Sanchez, F. Shen, A. Chen and J. Sheng, Chem. Commun., 2015, 51, 16369 DOI: 10.1039/C5CC07479G

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