Multiple MoS2 Transistors for Sensing Molecule Interaction Kinetics

Atomically layered transition metal dichalcogenides (TMDCs) exhibit a significant potential to enable next-generation low-cost transistor biosensors that permit single-molecule-level quantification of biomolecules. To realize such potential biosensing capability, device-oriented research is needed f...

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Published inScientific reports Vol. 5; no. 1; p. 10546
Main Authors Nam, Hongsuk, Oh, Bo-Ram, Chen, Pengyu, Chen, Mikai, Wi, Sungjin, Wan, Wenjie, Kurabayashi, Katsuo, Liang, Xiaogan
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 27.05.2015
Nature Publishing Group
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Summary:Atomically layered transition metal dichalcogenides (TMDCs) exhibit a significant potential to enable next-generation low-cost transistor biosensors that permit single-molecule-level quantification of biomolecules. To realize such potential biosensing capability, device-oriented research is needed for calibrating the sensor responses to enable the quantification of the affinities/kinetics of biomolecule interactions. In this work, we demonstrated MoS 2 -based transistor biosensors capable of detecting tumor necrosis factor – alpha (TNF-α) with a detection limit as low as 60 fM. Such a detection limit was achieved in both linear and subthreshold regimes of MoS 2 transistors. In both regimes, all sets of transistors exhibited consistent calibrated responses with respect to TNF-α concentration and they resulted in a standard curve, from which the equilibrium constant of the antibody-(TNF-α) pair was extracted to be K D  = 369 ± 48 fM. Based on this calibrated sensor model, the time-dependent binding kinetics was also measured and the association/dissociation rates of the antibody-(TNF-α) pair were extracted to be (5.03 ± 0.16) × 10 8  M −1 s −1 and (1.97 ± 0.08) × 10 −4  s −1 , respectively. This work advanced the critical device physics for leveraging the excellent electronic/structural properties of TMDCs in biosensing applications as well as the research capability in analyzing the biomolecule interactions with fM-level sensitivities.
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These authors contributed equally to this work.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep10546