Structure of hydrated oligonucleotides studied by in situ scanning tunneling microscopy

T. W. Jing, A. M. Jeffrey, J. A. DeRose, Y. L. Lyubchenko, L. S. Shlyakhtenko, R. E. Harrington, E. Appella, J. Larsen, A. Vaught, D. Rekesh, F. X. Lu, S. M. Lindsay

Research output: Contribution to journalArticle

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Abstract

We have used the scanning tunneling microscope (STM) to image several synthetic oligonucleotides adsorbed onto a positively charged Au(111) electrode. The molecules were deposited and imaged in aqueous electrolyte under potential control, a procedure that eliminated the problem of the substrate artifacts that had limited some previous STM studies. Experiments were carried out with two types of single-stranded molecules (11 and 20 bases long) and three types of double-stranded molecules (20 and 61 base pairs and 31 bases with 25 bases paired and 6-base "sticky" ends). The molecules lie along symmetry directions on the reconstructed (23 x √3) gold surface, and length measurements indicate that they adopt simple base-stacked structures. The base stacking distances are, within experimental uncertainty, equal to the 0.33 nm measured for polymeric aggregates of stacked purines by direct imaging in identical conditions. The images show features consistent with helical structures. Double helices have a major-groove periodicity that is consistent with a 36° twist. The single helices appear to be more tightly twisted. A simple tunneling model of STM contrast generates good agreement between measured and calculated images.

Original languageEnglish (US)
Pages (from-to)8934-8938
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume90
Issue number19
DOIs
StatePublished - Oct 1 1993

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Scanning Tunnelling Microscopy
Purines
Periodicity
Oligonucleotides
Base Pairing
Gold
Artifacts
Electrolytes
Uncertainty
Electrodes
Direction compound

ASJC Scopus subject areas

  • General

Cite this

Structure of hydrated oligonucleotides studied by in situ scanning tunneling microscopy. / Jing, T. W.; Jeffrey, A. M.; DeRose, J. A.; Lyubchenko, Y. L.; Shlyakhtenko, L. S.; Harrington, R. E.; Appella, E.; Larsen, J.; Vaught, A.; Rekesh, D.; Lu, F. X.; Lindsay, S. M.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 90, No. 19, 01.10.1993, p. 8934-8938.

Research output: Contribution to journalArticle

Jing, TW, Jeffrey, AM, DeRose, JA, Lyubchenko, YL, Shlyakhtenko, LS, Harrington, RE, Appella, E, Larsen, J, Vaught, A, Rekesh, D, Lu, FX & Lindsay, SM 1993, 'Structure of hydrated oligonucleotides studied by in situ scanning tunneling microscopy', Proceedings of the National Academy of Sciences of the United States of America, vol. 90, no. 19, pp. 8934-8938. https://doi.org/10.1073/pnas.90.19.8934
Jing, T. W. ; Jeffrey, A. M. ; DeRose, J. A. ; Lyubchenko, Y. L. ; Shlyakhtenko, L. S. ; Harrington, R. E. ; Appella, E. ; Larsen, J. ; Vaught, A. ; Rekesh, D. ; Lu, F. X. ; Lindsay, S. M. / Structure of hydrated oligonucleotides studied by in situ scanning tunneling microscopy. In: Proceedings of the National Academy of Sciences of the United States of America. 1993 ; Vol. 90, No. 19. pp. 8934-8938.
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