Kissing interactions for the design of a multicolour fluorescence anisotropy chiral aptasensor

The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the s...

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Vydáno v:Talanta (Oxford) Ročník 205; s. 120098
Hlavní autoři: Chovelon, Benoit, Fiore, Emmanuelle, Faure, Patrice, Peyrin, Eric, Ravelet, Corinne
Médium: Journal Article
Jazyk:angličtina
Vydáno: Netherlands Elsevier B.V 01.12.2019
Elsevier
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ISSN:0039-9140, 1873-3573, 1873-3573
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Abstract The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the simultaneous enantiomer quantification and the enantiopurity analysis. D- and L-arginine vasopressin (AVP) were employed as model enantiomeric targets. The D- and L-AVP engineered aptamers (aptaswitch) were used as recognition units whereas the Fluorescein or Texas Red labelled D- and L-hairpin probes (aptakiss) served as probes of the enantiomer-dependent AKC formation. The orthogonal fluorescence anisotropy signaling scheme at two different emission wavelengths permitted the concomitant sensing of the AVP enantiomers in a single sample, under a high-throughput microplate format. It was also shown that the AKC-based enantioselective sensor allowed the enantiomeric impurity detection at a level as low as 0.01%. [Display omitted] •A orthogonal fluorescence anisotropy chiral aptasensor was reported.•The enantioselective assay principle was based on the aptamer kissing complex strategy.•The aptasensor provided the concomitant detection of oligopeptide enantiomers in the same sample.•An enantiomeric impurity of as low as 0.01% was detected in a non racemic mixture.
AbstractList The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the simultaneous enantiomer quantification and the enantiopurity analysis. D- and L-arginine vasopressin (AVP) were employed as model enantiomeric targets. The D- and L-AVP engineered aptamers (aptaswitch) were used as recognition units whereas the Fluorescein or Texas Red labelled D- and L-hairpin probes (aptakiss) served as probes of the enantiomer-dependent AKC formation. The orthogonal fluorescence anisotropy signaling scheme at two different emission wavelengths permitted the concomitant sensing of the AVP enantiomers in a single sample, under a high-throughput microplate format. It was also shown that the AKC-based enantioselective sensor allowed the enantiomeric impurity detection at a level as low as 0.01%.The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the simultaneous enantiomer quantification and the enantiopurity analysis. D- and L-arginine vasopressin (AVP) were employed as model enantiomeric targets. The D- and L-AVP engineered aptamers (aptaswitch) were used as recognition units whereas the Fluorescein or Texas Red labelled D- and L-hairpin probes (aptakiss) served as probes of the enantiomer-dependent AKC formation. The orthogonal fluorescence anisotropy signaling scheme at two different emission wavelengths permitted the concomitant sensing of the AVP enantiomers in a single sample, under a high-throughput microplate format. It was also shown that the AKC-based enantioselective sensor allowed the enantiomeric impurity detection at a level as low as 0.01%.
The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the simultaneous enantiomer quantification and the enantiopurity analysis. D- and L-arginine vasopressin (AVP) were employed as model enantiomeric targets. The D- and L-AVP engineered aptamers (aptaswitch) were used as recognition units whereas the Fluorescein or Texas Red labelled D- and L-hairpin probes (aptakiss) served as probes of the enantiomer-dependent AKC formation. The orthogonal fluorescence anisotropy signaling scheme at two different emission wavelengths permitted the concomitant sensing of the AVP enantiomers in a single sample, under a high-throughput microplate format. It was also shown that the AKC-based enantioselective sensor allowed the enantiomeric impurity detection at a level as low as 0.01%.
The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated that the previously reported aptamer kissing complex (AKC) assay strategy can be implemented for designing a chiral tool that allows both the simultaneous enantiomer quantification and the enantiopurity analysis. D- and L-arginine vasopressin (AVP) were employed as model enantiomeric targets. The D- and L-AVP engineered aptamers (aptaswitch) were used as recognition units whereas the Fluorescein or Texas Red labelled D- and L-hairpin probes (aptakiss) served as probes of the enantiomer-dependent AKC formation. The orthogonal fluorescence anisotropy signaling scheme at two different emission wavelengths permitted the concomitant sensing of the AVP enantiomers in a single sample, under a high-throughput microplate format. It was also shown that the AKC-based enantioselective sensor allowed the enantiomeric impurity detection at a level as low as 0.01%. [Display omitted] •A orthogonal fluorescence anisotropy chiral aptasensor was reported.•The enantioselective assay principle was based on the aptamer kissing complex strategy.•The aptasensor provided the concomitant detection of oligopeptide enantiomers in the same sample.•An enantiomeric impurity of as low as 0.01% was detected in a non racemic mixture.
ArticleNumber 120098
Author Fiore, Emmanuelle
Ravelet, Corinne
Chovelon, Benoit
Faure, Patrice
Peyrin, Eric
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  givenname: Eric
  surname: Peyrin
  fullname: Peyrin, Eric
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  givenname: Corinne
  surname: Ravelet
  fullname: Ravelet, Corinne
  email: corinne.ravelet@univ-grenoble-alpes.fr
  organization: University Grenoble Alpes, DPM UMR 5063, F-38041 Grenoble, CNRS, DPM UMR 5063, F-38041, Grenoble, France
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Keywords Orthogonal detection
Fluorescence anisotropy
Aptamer kissing complex
Enantiomeric purity
Language English
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Snippet The development of enantioselective assays and sensors has received much attention for the determination of enantiomeric impurities. Herein, we demonstrated...
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SubjectTerms anisotropy
Aptamer kissing complex
aptasensors
arginine
Chemical Sciences
Enantiomeric purity
enantiomers
enantioselectivity
fluorescein
fluorescence
Fluorescence anisotropy
oligonucleotides
Orthogonal detection
vasopressin
wavelengths
Title Kissing interactions for the design of a multicolour fluorescence anisotropy chiral aptasensor
URI https://dx.doi.org/10.1016/j.talanta.2019.06.098
https://www.ncbi.nlm.nih.gov/pubmed/31450392
https://www.proquest.com/docview/2281101653
https://www.proquest.com/docview/2286848328
https://hal.science/hal-03487365
Volume 205
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