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Direct digital sensing of protein biomarkers in solution

Author

Listed:
  • Georg Krainer

    (University of Cambridge)

  • Kadi L. Saar

    (University of Cambridge)

  • William E. Arter

    (University of Cambridge)

  • Timothy J. Welsh

    (University of Cambridge)

  • Magdalena A. Czekalska

    (University of Cambridge
    Unit A The Paddocks Business Centre)

  • Raphaël P. B. Jacquat

    (University of Cambridge)

  • Quentin Peter

    (University of Cambridge)

  • Walther C. Traberg

    (University of Cambridge)

  • Arvind Pujari

    (University of Cambridge
    University of Cambridge)

  • Akhila K. Jayaram

    (University of Cambridge)

  • Pavankumar Challa

    (University of Cambridge)

  • Christopher G. Taylor

    (University of Cambridge)

  • Lize-Mari Linden

    (Technische Universität Dresden)

  • Titus Franzmann

    (Technische Universität Dresden)

  • Roisin M. Owens

    (University of Cambridge)

  • Simon Alberti

    (Technische Universität Dresden)

  • David Klenerman

    (University of Cambridge)

  • Tuomas P. J. Knowles

    (University of Cambridge
    University of Cambridge)

Abstract

The detection of proteins is of central importance to biomolecular analysis and diagnostics. Typical immunosensing assays rely on surface-capture of target molecules, but this constraint can limit specificity, sensitivity, and the ability to obtain information beyond simple concentration measurements. Here we present a surface-free, single-molecule microfluidic sensing platform for direct digital protein biomarker detection in solution, termed digital immunosensor assay (DigitISA). DigitISA is based on microchip electrophoretic separation combined with single-molecule detection and enables absolute number/concentration quantification of proteins in a single, solution-phase step. Applying DigitISA to a range of targets including amyloid aggregates, exosomes, and biomolecular condensates, we demonstrate that the assay provides information beyond stoichiometric interactions, and enables characterization of immunochemistry, binding affinity, and protein biomarker abundance. Taken together, our results suggest a experimental paradigm for the sensing of protein biomarkers, which enables analyses of targets that are challenging to address using conventional immunosensing approaches.

Suggested Citation

  • Georg Krainer & Kadi L. Saar & William E. Arter & Timothy J. Welsh & Magdalena A. Czekalska & Raphaël P. B. Jacquat & Quentin Peter & Walther C. Traberg & Arvind Pujari & Akhila K. Jayaram & Pavankuma, 2023. "Direct digital sensing of protein biomarkers in solution," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-35792-x
    DOI: 10.1038/s41467-023-35792-x
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    References listed on IDEAS

    as
    1. Christoph J. Wienken & Philipp Baaske & Ulrich Rothbauer & Dieter Braun & Stefan Duhr, 2010. "Protein-binding assays in biological liquids using microscale thermophoresis," Nature Communications, Nature, vol. 1(1), pages 1-7, December.
    2. Georg Krainer & Timothy J. Welsh & Jerelle A. Joseph & Jorge R. Espinosa & Sina Wittmann & Ella Csilléry & Akshay Sridhar & Zenon Toprakcioglu & Giedre Gudiškytė & Magdalena A. Czekalska & William E. , 2021. "Reentrant liquid condensate phase of proteins is stabilized by hydrophobic and non-ionic interactions," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
    3. David A. Giljohann & Chad A. Mirkin, 2009. "Drivers of biodiagnostic development," Nature, Nature, vol. 462(7272), pages 461-464, November.
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    Cited by:

    1. Mrityunjoy Kar & Laura T. Vogel & Gaurav Chauhan & Suren Felekyan & Hannes Ausserwöger & Timothy J. Welsh & Furqan Dar & Anjana R. Kamath & Tuomas P. J. Knowles & Anthony A. Hyman & Claus A. M. Seidel, 2024. "Solutes unmask differences in clustering versus phase separation of FET proteins," Nature Communications, Nature, vol. 15(1), pages 1-21, December.

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