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Instantaneous Detection of αs-Casein in Cow’s Milk Using Fluorogenic Peptide Aptamers


The most abundant protein in cow’s milk is αs-casein, which is an allergen responsible for causing allergic reactions, including the life-threatening, hyper-sensitive immune reaction anaphylaxis. Casein sensors are used widely to avoid its ingestion or food contamination; however, these sensors use expensive antibodies and require several tens of minutes to process the multiple steps required for analysis. To overcome these drawbacks, we used fluorogenic peptide aptamers that instantaneously enhance their fluorescence upon binding to a target molecule. Two fluorogenic peptide aptamers, Cas1 and Cas2, were selected using ribosome display. Both aptamers instantaneously enhanced their fluorescence in the presence of αs-casein. Modification at the N-terminus of Cas1 with polyethylene glycol (PEG-cas1) suppresses fluorescence enhancement for a negative control protein, β-lactoglobulin, presumably because the modification suppresses unwanted interactions between PEG-cas1 and β-lactoglobulin. The detection limit of our fluorogenic aptamer system was found to be ~1 ppm, which is comparable with that of commercially available immunochromatography kits for αs-casein. Notably, our system can detect αs-casein in an exceptionally short time (i.e., 20–25 s) when compared with the 15 min required by immunochromatography kits. We also demonstrated that the prompt fluorescence enhancement of PEG-cas1 in the presence of αs-casein can be observed even by our naked eyes. The results of this study demonstrate the remarkable ability of fluorogenic aptamers and their potential application for other target molecules.

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Article information

26 Nov 2019
22 Jan 2020
First published
22 Jan 2020

Anal. Methods, 2020, Accepted Manuscript
Article type

Instantaneous Detection of αs-Casein in Cow’s Milk Using Fluorogenic Peptide Aptamers

C. Phadke, S. Tada, I. Kono, A. Hiyama, Y. Takase, S. Gayama, T. Aigaki, Y. Ito and T. UZAWA, Anal. Methods, 2020, Accepted Manuscript , DOI: 10.1039/C9AY02542A

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