Evidence map›Paper›PMID 24926389›Full record

ArticleBiomicrofluidics2014

Single cell kinase signaling assay using pinched flow coupled droplet microfluidics.

Ramesh Ramji, Ming Wang, Ali Asgar S Bhagat, Daniel Tan Shao Weng, Nitish V Thakor, Chwee Teck Lim, Chia-Hung Chen

Open access · hybridAbstract read
In one paragraph

Article in Biomicrofluidics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.9field-weighted citation impact, top 10% of its field
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

13 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Counting Proteins in Single Cells with Addressable Droplet Microarrays.Journal of visualized experiments : JoVE · 2018
    Article
  7. Review
  8. Microfluidics in systems biology-hype or truly useful?Current opinion in biotechnology · 2016
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
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

7 authors at 2 institutions in 1 country.

Ramesh RamjiDepartment of Biomedical Engineering, National University of Singapore, Singapore 117575.
Ming WangDepartment of Biomedical Engineering, National University of Singapore, Singapore 117575.
Ali Asgar S BhagatClearbridge Biomedics Pte. Ltd., Singapore 118257.
Daniel Tan Shao WengNational Cancer Centre Singapore, Singapore 169610.
Nitish V ThakorDepartment of Biomedical Engineering, National University of Singapore, Singapore 117575 ; Singapore Institute for Neurotechnology, Singapore 117456.
Chwee Teck LimDepartment of Biomedical Engineering, National University of Singapore, Singapore 117575 ; Department of Mechanical Engineering, National University of Singapore, Singapore 117575.
Chia-Hung ChenDepartment of Biomedical Engineering, National University of Singapore, Singapore 117575 ; Singapore Institute for Neurotechnology, Singapore 117456.
National University of Singapore · SGNational Cancer Centre Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Droplet-based microfluidics has shown potential in high throughput single cell assays by encapsulating individual cells in water-in-oil emulsions. Ordering cells in a micro-channel is necessary to encapsulate individual cells into droplets further enhancing the assay efficiency. This is typically limited due to the difficulty of preparing high-density cell solutions and maintaining them without cell aggregation in long channels (>5 cm). In this study, we developed a short pinched flow channel (5 mm) to separate cell aggregates and to form a uniform cell distribution in a droplet-generating platform that encapsulated single cells with >55% encapsulation efficiency beating Poisson encapsulation statistics. Using this platform and commercially available Sox substrates (8-hydroxy-5-(N,N-dimethylsulfonamido)-2-methylquinoline), we have demonstrated a high throughput dynamic single cell signaling assay to measure the activity of receptor tyrosine kinases (RTKs) in lung cancer cells triggered by cell surface ligand binding. The phosphorylation of the substrates resulted in fluorescent emission, showing a sigmoidal increase over a 12 h period. The result exhibited a heterogeneous signaling rate in individual cells and showed various levels of drug resistance when treated with the tyrosine kinase inhibitor, gefitinib.

Identifiers

PMID24926389
PMCPMC4032411
OpenAlexW2027906919

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.