| Literature DB >> 32893612 |
Mingfu Chen1, Chloé Grazon2,3, Prerana Sensharma1, Thuy T Nguyen1, Yunpeng Feng1, Margaret Chern1, R C Baer4, Nitinun Varongchayakul1, Katherine Cook2, Sébastien Lecommandoux3, Catherine M Klapperich1,5, James E Galagan1,4, Allison M Dennis1,5, Mark W Grinstaff1,2,5.
Abstract
Immobilization of biosensors in or on a functional material is critical for subsequent device development and translation to wearable technology. Here, we present the development and assessment of an immobilized quantum dot-transcription factor-nucleic acid complex for progesterone detection as a first step toward such device integration. The sensor, composed of a polyhistidine-tagged transcription factor linked to a quantum dot and a fluorophore-modified cognate DNA, is embedded within a hydrogel as an immobilization matrix. The hydrogel is optically transparent, soft, and flexible as well as traps the quantum dot-transcription factor DNA assembly but allows free passage of the analyte, progesterone. Upon progesterone exposure, DNA dissociates from the quantum dot-transcription factor DNA assembly resulting in an attenuated ratiometric fluorescence output via Förster resonance energy transfer. The sensor performs in a dose-dependent manner with a limit of detection of 55 nM. Repeated analyte measurements are similarly successful. Our approach combines a systematically characterized hydrogel as an immobilization matrix and a transcription factor-DNA assembly as a recognition/transduction element, offering a promising framework for future biosensor devices.Entities:
Keywords: Förster resonance energy transfer; biosensing; hydrogel; quantum dots; transcription factor
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Year: 2020 PMID: 32893612 DOI: 10.1021/acsami.0c13489
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229