Evidence map›Paper›PMID 36421154›Full record

ArticleBiosensors2022

On-Chip Single-Cell Bioelectrical Analysis for Identification of Cell Electrical Phenotyping in Response to Sequential Electric Signal Modulation.

Seungyeop Choi, Insu Park, Sang Hyun Lee, Kang In Yeo, Gyeongjun Min, Sung-Hun Woo, Yoon Suk Kim, Sei Young Lee, Sang Woo Lee

Abstract read
In one paragraph

Article in Biosensors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Seungyeop ChoiDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.ORCID 0000-0002-3192-579X
Insu ParkHolonyak Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.ORCID 0000-0002-3229-8345
Sang Hyun LeeDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.ORCID 0000-0003-2400-8720
Kang In YeoDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.
Gyeongjun MinDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.
Sung-Hun WooDepartment of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.ORCID 0000-0002-1642-9341
Yoon Suk KimDepartment of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
Sei Young LeeDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.
Sang Woo LeeDepartment of Biomedical Engineering, Yonsei University, Wonju 26493, Republic of Korea.

Funding

National Research Foundation of Korea NRF-2021R1A6A3A01086768National Research Foundation of Korea NRF-2021R1F1A1046496
6 · The paper itself

Abstract

In recent years, an interesting biomarker called membrane breakdown voltage has been examined using artificial planar lipid bilayers. Even though they have great potential to identify cell electrical phenotyping for distinguishing similar cell lines or cells under different physiological conditions, the biomarker has not been evaluated in the context of living cell electrical phenotyping. Herein, we present a single-cell analysis platform to continuously measure the electric response in a large number of cells in parallel using electric frequency and voltage variables. Using this platform, we measured the direction of cell displacement and transparent cell image alteration as electric polarization of the cell responds to signal modulation, extracting the dielectrophoretic crossover frequency and membrane breakdown voltage for each cell, and utilizing the measurement results in the same spatiotemporal environment. We developed paired parameters using the dielectrophoretic crossover frequency and membrane breakdown voltage for each cell and evaluated the paired parameter efficiency concerning the identification of two different breast cancer cells and cell drug response. Moreover, we showed that the platform was able to identify cell electrical phenotyping, which was generated by subtle changes in cholesterol depletion-induced cell membrane integrity disruption when the paired parameter was used. Our platform introduced in this paper is extremely useful for facilitating more accurate and efficient evaluation of cell electrical phenotyping in a variety of applications, such as cell biology and drug discovery.

Indexed as

Lipid BilayersSingle-Cell AnalysisCell MembraneElectricityLipid BilayersDEP crossover frequencydielectrophoresiselectrical phenotypeelectroporationmembrane breakdown

Identifiers

PMID36421154
PMCPMC9688586

What OpenQuestion holds

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Registered trials

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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.