Evidence map›Paper›PMID 35733793›Full record

ArticleiScience2022

High-throughput single-cell antibody secretion quantification and enrichment using droplet microfluidics-based FRET assay.

Justina Rutkauskaite, Simon Berger, Stavros Stavrakis, Oliver Dressler, John Heyman, Xavier Casadevall I Solvas, Andrew deMello, Linas Mazutis

Abstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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  11. Article
  12. Fluorescence-activated droplet sequencing (FAD-seq) directly provides sequences of screening hits in antibody discovery.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Deciphering the aging process through single-cell cytometric technologies.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2024
    Review
  14. Directed evolution of material-producing microorganisms.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Justina RutkauskaiteInstitute of Biotechnology, Life Sciences Centre, Vilnius University, 7 Sauletekio ave., 10257 Vilnius, Lithuania.
Simon BergerInstitute for Chemical and Bioengineering, ETH Zurich, Vladimir Prelog Weg 1, 8093 Zürich, Switzerland.
Stavros StavrakisInstitute for Chemical and Bioengineering, ETH Zurich, Vladimir Prelog Weg 1, 8093 Zürich, Switzerland.
Oliver DresslerInstitute for Chemical and Bioengineering, ETH Zurich, Vladimir Prelog Weg 1, 8093 Zürich, Switzerland.
John HeymanHarvard University, SEAS, 9 Oxford St., Cambridge, MA 02139, USA.
Xavier Casadevall I SolvasMeBioS division, Department of Biosystems, KU Leuven, Willem de Croylaan 42, 3001 Leuven, Belgium.
Andrew deMelloInstitute for Chemical and Bioengineering, ETH Zurich, Vladimir Prelog Weg 1, 8093 Zürich, Switzerland.
Linas MazutisInstitute of Biotechnology, Life Sciences Centre, Vilnius University, 7 Sauletekio ave., 10257 Vilnius, Lithuania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput screening and enrichment of antibody-producing cells have many important applications. Herein, we present a droplet microfluidic approach for high-throughput screening and sorting of antibody-secreting cells using a Förster resonance electron transfer (FRET)-based assay. The FRET signal is mediated by the specific binding of the secreted antibody to two fluorescently labeled probes supplied within a droplet. Functional hybridoma cells expressing either membrane-bound or secreted monoclonal antibodies (mAbs), or both, were efficiently differentiated in less than 30 min. The antibody secretion rate by individual hybridoma cells was recorded in the range of 14,000 Abs/min, while the density of membrane-bound fraction was approximately 100 Abs/μm

Indexed as

Biological sciencesBiotechnologyImmunological methodsImmunology

Identifiers

PMID35733793
PMCPMC9207670

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.