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Aptamer−DNAzyme Hairpins for Amplified Biosensing

Teller, Carsten, Shimron, Simcha, Willner, Itamar·2009·Analytical Chemistry

Abstract

Engineered nucleic acid hairpin structures are used for the amplified analysis of low-molecular-weight substrates (adenosine monophosphate, AMP) or proteins (lysozyme). The hairpin structures consist of the anti-AMP or antilysozyme aptamer units linked to the horseradish peroxidase (HRP)-mimicking DNAzyme sequence. The HRP-mimicking DNAzyme sequence is protected in a "caged", inactive structure in the stem regions of the respective hairpins, whereas the loop regions include a part of the respective aptamer sequence. The opening of the hairpins by the analytes, AMP or lysozyme, through the formation of the respective analyte-aptamer complexes, results in the self-assembly of the active HRP-mimicking DNAzyme. The DNAzyme catalyzes the H(2)O(2)-mediated oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS(2-)) to the colored ABTS(*-), thus providing the amplified optical detection of the respective analytes. The engineered aptamer-DNAzyme hairpin structures reveal significantly improved analytical performance, as compared to analogous fluorophore-quencher-labeled hairpins.

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Metadata

Authors
Teller, C., Shimron, S., & Willner, I.
Venue
Analytical Chemistry
Published
2009-09-25
Volume
81
Issue
21
Pages
9114-9119
ISSN
  • 0003-2700 (ISSN-L)
  • 1520-6882
OpenAlex
W2017815617
Cited by
199
References
0
FWCI
8.88
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Aptamer−DNAzyme Hairpins for Amplified Biosensing. https://app.cochat.ai/papers/10.1021/ac901773b
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Teller, C., Shimron, S., & Willner, I. (2009). Aptamer−DNAzyme Hairpins for Amplified Biosensing. Analytical Chemistry. https://doi.org/10.1021/ac901773b

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