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1.
Nat Commun ; 10(1): 3712, 2019 08 16.
Artigo em Inglês | MEDLINE | ID: mdl-31420559

RESUMO

Nanopore-based single nanoparticle detection has recently emerged as a vibrant research field with numerous high-impact applications. Here, we introduce a programmable optofluidic chip for nanopore-based particle analysis: feedback-controlled selective delivery of a desired number of biomolecules and integration of optical detection techniques on nanopore-selected particles. We demonstrate the feedback-controlled introduction of individual biomolecules, including 70S ribosomes, DNAs and proteins into a fluidic channel where the voltage across the nanopore is turned off after a user-defined number of single molecular insertions. Delivery rates of hundreds/min with programmable off-times of the pore are demonstrated using individual 70S ribosomes. We then use real-time analysis of the translocation signal for selective voltage gating of specific particles from a mixture, enabling selection of DNAs from a DNA-ribosome mixture. Furthermore, we report optical detection of nanopore-selected DNA molecules. These capabilities point the way towards a powerful research tool for high-throughput single-molecule analysis on a chip.


Assuntos
Dispositivos Lab-On-A-Chip , Nanoporos , Dispositivos Ópticos , Imagem Individual de Molécula/instrumentação , DNA , Escherichia coli , Ribossomos
2.
Optica ; 6(9): 1130-1131, 2019 Sep 20.
Artigo em Inglês | MEDLINE | ID: mdl-33598506

RESUMO

We use optical trapping to deliver molecular targets to the vicinity of a nanopore for high-throughput single molecule analysis on an optofluidic chip. DNA detection rates increase over 80× to enable detection at attomolar concentrations.

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