Synthesis, structure and imaging of oligodeoxyribonucleotides with tellurium-nucleobase derivatization

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Abstract

We report here the first synthesis of 5-phenyl-telluride-thymidine derivatives and the Te-phosphoramidite. We also report here the synthesis, structure and STM current-imaging studies of DNA oligonucleotides containing the nucleobases (thymine) derivatized with 5-phenyl-telluride functionality (5-Te). Our results show that the 5-Te-DNA is stable, and that the Te-DNA duplex has the thermo-stability similar to the corresponding native duplex. The crystal structure indicates that the 5-Te-DNA duplex structure is virtually identical to the native one, and that the Te-modified T and native A interact similarly to the native T and A pair. Furthermore, while the corresponding native showed weak signals, the DNA duplex modified with electron-rich tellurium functionality showed strong topographic and current peaks by STM imaging, suggesting a potential strategy to directly image DNA without structural perturbation. © 2011 The Author(s).

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Sheng, J., Hassan, A. E. A., Zhang, W., Zhou, J., Xu, B., Soares, A. S., & Huang, Z. (2011). Synthesis, structure and imaging of oligodeoxyribonucleotides with tellurium-nucleobase derivatization. Nucleic Acids Research, 39(9), 3962–3971. https://doi.org/10.1093/nar/gkq1288

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