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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Published in:	Talanta (Oxford) Vol. 205; p. 120098
Main Authors:	Chovelon, Benoit, Fiore, Emmanuelle, Faure, Patrice, Peyrin, Eric, Ravelet, Corinne
Format:	Journal Article
Language:	English
Published:	Netherlands Elsevier B.V 01.12.2019 Elsevier
Subjects:	anisotropy Aptamer kissing complex aptasensors arginine Chemical Sciences Enantiomeric purity enantiomers enantioselectivity fluorescein fluorescence Fluorescence anisotropy oligonucleotides Orthogonal detection vasopressin wavelengths Orthogonal detection Fluorescence anisotropy Aptamer kissing complex Enantiomeric purity
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
Author_xml	– sequence: 1 givenname: Benoit surname: Chovelon fullname: Chovelon, Benoit organization: University Grenoble Alpes, DPM UMR 5063, F-38041 Grenoble, CNRS, DPM UMR 5063, F-38041, Grenoble, France – sequence: 2 givenname: Emmanuelle surname: Fiore fullname: Fiore, Emmanuelle organization: University Grenoble Alpes, DPM UMR 5063, F-38041 Grenoble, CNRS, DPM UMR 5063, F-38041, Grenoble, France – sequence: 3 givenname: Patrice surname: Faure fullname: Faure, Patrice organization: Département de Biochimie, Toxicologie et Pharmacologie, CHU de Grenoble Site Nord - Institut de biologie et de pathologie, F-38041, Grenoble, France – sequence: 4 givenname: Eric surname: Peyrin fullname: Peyrin, Eric email: eric.peyrin@univ-grenoble-alpes.fr organization: University Grenoble Alpes, DPM UMR 5063, F-38041 Grenoble, CNRS, DPM UMR 5063, F-38041, Grenoble, France – sequence: 5 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
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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
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