Evidence map›Paper›PMID 35965781›Full record

ArticleeLight2022

Light-driven single-cell rotational adhesion frequency assay.

Yaoran Liu, Hongru Ding, Jingang Li, Xin Lou, Mingcheng Yang, Yuebing Zheng

Open access · diamondAbstract read
In one paragraph

Article in eLight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Optical sorting: past, present and future.Light, science & applications · 2025
    Review
  7. Article
  8. Article
  9. Light-controlled soft bio-microrobot.Light, science & applications · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Optothermal rotation of micro-/nano-objects.Chemical communications (Cambridge, England) · 2023
    Review
  14. Article
  15. Article
  16. Light-driven high-precision cell adhesion kinetics.Light, science & applications · 2022
    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

6 authors at 4 institutions in 2 countries.

Yaoran LiuDepartment of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX 78712 USA.
Hongru DingWalker Department of Mechanical Engineering, The University of Texas at Austin, Austin, TX 78712 USA.
Jingang LiMaterials Science & Engineering Program and Texas Materials Institute, The University of Texas at Austin, Austin, TX 78712 USA.
Xin LouSchool of Physical Sciences, University of Chinese Academy of Sciences, Beijing, 100049 China.
Mingcheng YangSchool of Physical Sciences, University of Chinese Academy of Sciences, Beijing, 100049 China.
Yuebing ZhengDepartment of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX 78712 USA.ORCID 0000-0002-9168-9477
The University of Texas at Austin · USChinese Academy of Sciences · CNUniversity of Chinese Academy of Sciences · CNWalker (United States) · US

Funding

On-Chip Multiplexed Adhesion Frequency Assay for Measuring Receptor-Ligand Interactions on CellsDP2GM128446 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI ZHENG, YUEBING · 2017 to 2017
$2.2M
NIGMS NIH HHS DP2 GM128446
6 · The paper itself

Abstract

The interaction between cell surface receptors and extracellular ligands is highly related to many physiological processes in living systems. Many techniques have been developed to measure the ligand-receptor binding kinetics at the single-cell level. However, few techniques can measure the physiologically relevant shear binding affinity over a single cell in the clinical environment. Here, we develop a new optical technique, termed single-cell rotational adhesion frequency assay (scRAFA), that mimics in vivo cell adhesion to achieve label-free determination of both homogeneous and heterogeneous binding kinetics of targeted cells at the subcellular level. Moreover, the scRAFA is also applicable to analyze the binding affinities on a single cell in native human biofluids. With its superior performance and general applicability, scRAFA is expected to find applications in study of the spatial organization of cell surface receptors and diagnosis of infectious diseases. Supplementary Information: The online version contains supplementary material available at 10.1186/s43593-022-00020-4.

Identifiers

PMID35965781
PMCPMC9358104
OpenAlexW4290471340

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.