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Nucleobase orientation and ordering in films of single-stranded DNA on gold.

Identifieur interne : 000391 ( Ncbi/Curation ); précédent : 000390; suivant : 000392

Nucleobase orientation and ordering in films of single-stranded DNA on gold.

Auteurs : Dmitri Y. Petrovykh [États-Unis] ; V. Pérez-Dieste ; Aric Opdahl ; Hiromi Kimura-Suda ; J M Sullivan ; Michael J. Tarlov ; F J Himpsel ; Lloyd J. Whitman

Source :

RBID : pubmed:16390092

Descripteurs français

English descriptors

Abstract

We demonstrate how the orientation and ordering of DNA bases in ultrahigh vacuum (UHV) and ambient environments can be determined using complementary spectroscopic methods. Near-edge X-ray absorption fine structure (NEXAFS) with fluorescence detection, X-ray photoelectron (XPS), and Fourier transform infrared (FTIR) spectroscopies are used to quantify the coverage, chemical composition, orientation, and ordering of thymine bases in model self-assembled monolayers of thymine homo-oligonucleotides [oligo(dT)] on gold. We find that, in monolayers of thiol-modified oligo(dT), thymine bases tend to orient parallel to the Au substrate, and this preferential orientation is significantly more pronounced in monolayers of thiolated 5-mers compared to 25-mers. We interpret this preferential orientation as a signature of significant correlations (local ordering) between individual nuleobases, which offers a way to quantify and compare nucleobase interactions in films under both ambient and UHV conditions.

DOI: 10.1021/ja052443e
PubMed: 16390092

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Le document en format XML

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<term>Oligodeoxyribonucleotides (chemistry)</term>
<term>Spectroscopy, Fourier Transform Infrared (methods)</term>
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<term>Oligodésoxyribonucléotides ()</term>
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<div type="abstract" xml:lang="en">We demonstrate how the orientation and ordering of DNA bases in ultrahigh vacuum (UHV) and ambient environments can be determined using complementary spectroscopic methods. Near-edge X-ray absorption fine structure (NEXAFS) with fluorescence detection, X-ray photoelectron (XPS), and Fourier transform infrared (FTIR) spectroscopies are used to quantify the coverage, chemical composition, orientation, and ordering of thymine bases in model self-assembled monolayers of thymine homo-oligonucleotides [oligo(dT)] on gold. We find that, in monolayers of thiol-modified oligo(dT), thymine bases tend to orient parallel to the Au substrate, and this preferential orientation is significantly more pronounced in monolayers of thiolated 5-mers compared to 25-mers. We interpret this preferential orientation as a signature of significant correlations (local ordering) between individual nuleobases, which offers a way to quantify and compare nucleobase interactions in films under both ambient and UHV conditions.</div>
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