IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v9y2018i1d10.1038_s41467-018-06345-4.html
   My bibliography  Save this article

Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity

Author

Listed:
  • Francesco Simone Ruggeri

    (University of Cambridge)

  • Jerome Charmet

    (University of Cambridge
    WMG, University of Warwick)

  • Tadas Kartanas

    (University of Cambridge)

  • Quentin Peter

    (University of Cambridge)

  • Sean Chia

    (University of Cambridge)

  • Johnny Habchi

    (University of Cambridge)

  • Christopher M. Dobson

    (University of Cambridge)

  • Michele Vendruscolo

    (University of Cambridge)

  • Tuomas P. J. Knowles

    (University of Cambridge
    University of Cambridge)

Abstract

Scanning probe microscopy provides a unique window into the morphology, mechanics, and structure of proteins and their complexes on the nanoscale. Such measurements require, however, deposition of samples onto substrates. This process can affect conformations and assembly states of the molecular species under investigation and can bias the molecular populations observed in heterogeneous samples through differential adsorption. Here, we show that these limitations can be overcome with a single-step microfluidic spray deposition platform. This method transfers biological solutions to substrates as microdroplets with subpicoliter volume, drying in milliseconds, a timescale that is shorter than typical diffusion times of proteins on liquid–solid interfaces, thus avoiding surface mass transport and change to the assembly state. Finally, the single-step deposition ensures the attachment of the full molecular content of the sample to the substrate, allowing quantitative measurements of different molecular populations within heterogeneous systems, including protein aggregates.

Suggested Citation

  • Francesco Simone Ruggeri & Jerome Charmet & Tadas Kartanas & Quentin Peter & Sean Chia & Johnny Habchi & Christopher M. Dobson & Michele Vendruscolo & Tuomas P. J. Knowles, 2018. "Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06345-4
    DOI: 10.1038/s41467-018-06345-4
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-018-06345-4
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-018-06345-4?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06345-4. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.