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  Visualizing single-cell secretion dynamics with single protein sensitivity

McDonald, M. P., Gemeinhardt, A., König, K., Piliarik, M., Schaffer, S., Völkl, S., et al. (2018). Visualizing single-cell secretion dynamics with single protein sensitivity. Nano Letters, 18, 513-519. doi:10.1021/acs.nanolett.7b04494.

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 Creators:
McDonald, Matthew Paul1, Author           
Gemeinhardt, André1, Author           
König, Katharina1, 2, Author           
Piliarik, Marek1, Author           
Schaffer, Stefanie3, Author
Völkl, Simon3, Author
Mackensen, Andreas3, Author
Sandoghdar, Vahid1, 4, Author           
Affiliations:
1Sandoghdar Division, Max Planck Institute for the Science of Light, Max Planck Society, ou_2364722              
2International Max Planck Research School, Max Planck Institute for the Science of Light, Max Planck Society, Staudtstraße 2, 91058 Erlangen, DE, ou_2364697              
3 Department of Internal Medicine 5, Hematology and Oncology, Friedrich Alexander University Erlangen-Nuremberg, Ulmenweg 18, 91054 Erlangen, Germany, ou_persistent22              
4Sandoghdar Division, Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society, ou_3596674              

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Free keywords: cellular secretion; dynamics; imaging; iSCAT; label-free; single-protein
 Abstract: Cellular secretion of proteins into the extracellular environment is an essential mediator of critical biological mechanisms, including cell-to-cell communication, immunological response, targeted delivery, and differentiation. Here, we report a novel methodology that allows for the real-time detection and imaging of single unlabeled proteins that are secreted from individual living cells. This is accomplished via interferometric detection of scattered light (iSCAT) and is demonstrated with Laz388 cells, an Epstein Barr virus (EBV)-transformed B cell line. We find that single Laz388 cells actively secrete IgG antibodies at a rate of the order of 100 molecules per second. Intriguingly, we also find that other proteins and particles spanning ca. 100 kDa-1 MDa are secreted from the Laz388 cells in tandem with IgG antibody release, likely arising from EBV-related viral proteins. The technique is general and, as we show, can also be applied to studying the lysate of a single cell. Our results establish label-free iSCAT imaging as a powerful tool for studying the real-time exchange between cells and their immediate environment with single-protein sensitivity.

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Language(s): eng - English
 Dates: 2018-01-10
 Publication Status: Issued
 Pages: 7
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1021/acs.nanolett.7b04494
 Degree: -

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Title: Nano Letters
  Abbreviation : Nano Lett.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 18 Sequence Number: - Start / End Page: 513 - 519 Identifier: ISSN: 1530-6984
CoNE: https://pure.mpg.de/cone/journals/resource/110978984570403