Logic gates with different radixes have been constructed using a biologically active molecule, 2-(4'-N,N-dimethylaminophenyl)imidazo[4,5-b]pyridine (DMAPIP-b). Taking advantage of the multiple binding sites of the fluorophore, a series of different molecular logic gates are developed using fluorescence intensities at different wavelengths. The high emission of the molecule is drastically quenched in the presence of Fe(3+). It is regained by the addition of an equivalent amount of F(-). The fluorescence On-Off nature has been used to construct molecular full subtractor and molecular keypad lock system with Boolean logic. A ternary system is generated by considering three defined fluorescence intensities at particular wavelengths. The smooth dependency of emission intensities with analyte concentration is utilized to construct an infinite-valued fuzzy logic system. The fuzzy logic system is further coupled with a neuro-adaptation method to predict more accurately the dependency of molecular intensity on external inputs.
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http://dx.doi.org/10.1039/c5an01068c | DOI Listing |
Nat Nanotechnol
January 2025
Wallace H. Coulter Department of Biomedical Engineering, Georgia Tech College of Engineering and Emory School of Medicine, Atlanta, GA, USA.
The forward design of biosensors that implement Boolean logic to improve detection precision primarily relies on programming genetic components to control transcriptional responses. However, cell- and gene-free nanomaterials programmed with logical functions may present lower barriers for clinical translation. Here we report the design of activity-based nanosensors that implement AND-gate logic without genetic parts via bi-labile cyclic peptides.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Center for Quantum Information, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea and Division of Quantum Information Technology, KIST School, Korea University of Science and Technology, Seoul 02792, Korea.
High-dimensional multipartite entanglement plays a crucial role in quantum information science. However, existing schemes for generating such entanglement become complex and costly as the dimension of quantum units increases. In this Letter, we overcome the limitation by proposing a significantly enhanced linear optical heralded scheme that generates the d-level N-partite Greenberger-Horne-Zeilinger (GHZ) state with single-photon sources and linear operations.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Inria Paris, Quandela, 7 Rue Léonard de Vinci, 91300 Massy, France.
Given some group G of logical gates, for instance the Clifford group, what are the quantum encodings for which these logical gates can be implemented by simple physical operations, described by some physical representation of G? We study this question by constructing a general form of such encoding maps. For instance, we recover that the ⟦5,1,3⟧ and Steane codes admit transversal implementations of the binary tetrahedral and binary octahedral groups, respectively. For bosonic encodings, we show how to obtain the GKP and cat qudit encodings by considering the appropriate groups, and essentially the simplest physical implementations.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
Department of Physics, Harvard University, Cambridge, Massachusetts 02138, USA.
Quantum error correction is believed to be essential for scalable quantum computation, but its implementation is challenging due to its considerable space-time overhead. Motivated by recent experiments demonstrating efficient manipulation of logical qubits using transversal gates [Bluvstein et al., Nature (London) 626, 58 (2024)NATUAS0028-083610.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, People's Republic of China.
CRISPR-Cas-based technology, emerging as a leading platform for molecular assays, has been extensively researched and applied in bioanalysis. However, achieving simultaneous and highly sensitive detection of multiple nucleic acid targets remains a significant challenge for most current CRISPR-Cas systems. Herein, a CRISPR Cas12a based calibratable single particle counting-mediated biosensor was constructed for dual RNAs logic and ultra-sensitive detection in one tube based on DNA Tetrahedron (DTN)-interface supported fluorescent particle probes coupled with a novel synergistic cascaded strategy between CRISPR Cas13a system and strand displacement amplification (SDA).
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