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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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McDonald, Matthew Paul1, Autor           
Gemeinhardt, André1, Autor           
König, Katharina1, 2, Autor           
Piliarik, Marek1, Autor           
Schaffer, Stefanie3, Autor
Völkl, Simon3, Autor
Mackensen, Andreas3, Autor
Sandoghdar, Vahid1, 4, Autor           
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              
4Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164414              

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Schlagwörter: cellular secretion; dynamics; imaging; iSCAT; label-free; single-protein
 Zusammenfassung: 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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Sprache(n): eng - English
 Datum: 2018-01-10
 Publikationsstatus: Erschienen
 Seiten: 7
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1021/acs.nanolett.7b04494
 Art des Abschluß: -

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Titel: Nano Letters
  Kurztitel : Nano Lett.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Washington, DC : American Chemical Society
Seiten: - Band / Heft: 18 Artikelnummer: - Start- / Endseite: 513 - 519 Identifikator: ISSN: 1530-6984
CoNE: https://pure.mpg.de/cone/journals/resource/110978984570403