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On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device

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 an...

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Autores principales: Rahman, M., Stott, M. A., Harrington, M., Li, Y., Sampad, M. J. N., Lancaster, L., Yuzvinsky, T. D., Noller, H. F., Hawkins, A. R., Schmidt, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697697/
https://www.ncbi.nlm.nih.gov/pubmed/31420559
http://dx.doi.org/10.1038/s41467-019-11723-7
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author Rahman, M.
Stott, M. A.
Harrington, M.
Li, Y.
Sampad, M. J. N.
Lancaster, L.
Yuzvinsky, T. D.
Noller, H. F.
Hawkins, A. R.
Schmidt, H.
author_facet Rahman, M.
Stott, M. A.
Harrington, M.
Li, Y.
Sampad, M. J. N.
Lancaster, L.
Yuzvinsky, T. D.
Noller, H. F.
Hawkins, A. R.
Schmidt, H.
author_sort Rahman, M.
collection PubMed
description 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.
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spelling pubmed-66976972019-08-19 On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device Rahman, M. Stott, M. A. Harrington, M. Li, Y. Sampad, M. J. N. Lancaster, L. Yuzvinsky, T. D. Noller, H. F. Hawkins, A. R. Schmidt, H. Nat Commun Article 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. Nature Publishing Group UK 2019-08-16 /pmc/articles/PMC6697697/ /pubmed/31420559 http://dx.doi.org/10.1038/s41467-019-11723-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rahman, M.
Stott, M. A.
Harrington, M.
Li, Y.
Sampad, M. J. N.
Lancaster, L.
Yuzvinsky, T. D.
Noller, H. F.
Hawkins, A. R.
Schmidt, H.
On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title_full On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title_fullStr On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title_full_unstemmed On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title_short On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
title_sort on demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697697/
https://www.ncbi.nlm.nih.gov/pubmed/31420559
http://dx.doi.org/10.1038/s41467-019-11723-7
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