Evidence map›Paper›PMID 34838160›Full record

ArticleCell2021

Deciphering cell signaling networks with massively multiplexed biosensor barcoding.

Jr-Ming Yang, Wei-Yu Chi, Jessica Liang, Saki Takayanagi, Pablo A Iglesias, Chuan-Hsiang Huang

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 52 citations in OpenAlex.

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  11. Reconstructing Signaling Networks Using Biosensor Barcoding.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jr-Ming YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA. Electronic address: jyang38@jhmi.edu.
Wei-Yu ChiDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA.
Jessica LiangDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Saki TakayanagiXDBio Graduate Program, Johns Hopkins School of Medicine, MD 21205, USA.
Pablo A IglesiasDepartment of Electrical and Computer Engineering, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Chuan-Hsiang HuangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA. Electronic address: chuang29@jhmi.edu.
Johns Hopkins University · US

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI TZYY-CHOOU WU · 2003 to 2026
$53.5M
Deciphering the network structure of signaling dynamicsR01GM136711 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI HUANG, CHUAN-HSIANG · 2020 to 2024
$1.7M
Zeiss LSM780 Confocal Microscope for a Core FacilityS10OD016374 · OD · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2013 to 2013
$584k
Coupling of PI3K signaling and actin-based cytoskeletal networks in cancer cell migration and metastasis?.K22CA212060 · NCI · JOHNS HOPKINS UNIVERSITY · PI HUANG, CHUAN-HSIANG · 2017 to 2019
$455k
LSM880 Laser-scanning Microscope with Airyscan ModuleS10OD023548 · OD · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2018 to 2018
$439k
NCI NIH HHS K22 CA212060NCI NIH HHS P50 CA098252NIGMS NIH HHS R01 GM136711NIH HHS S10 OD016374NIH HHS S10 OD023548
6 · The paper itself

Abstract

Genetically encoded fluorescent biosensors are powerful tools for monitoring biochemical activities in live cells, but their multiplexing capacity is limited by the available spectral space. We overcome this problem by developing a set of barcoding proteins that can generate over 100 barcodes and are spectrally separable from commonly used biosensors. Mixtures of barcoded cells expressing different biosensors are simultaneously imaged and analyzed by deep learning models to achieve massively multiplexed tracking of signaling events. Importantly, different biosensors in cell mixtures show highly coordinated activities, thus facilitating the delineation of their temporal relationship. Simultaneous tracking of multiple biosensors in the receptor tyrosine kinase signaling network reveals distinct mechanisms of effector adaptation, cell autonomous and non-autonomous effects of KRAS mutations, as well as complex interactions in the network. Biosensor barcoding presents a scalable method to expand multiplexing capabilities for deciphering the complexity of signaling networks and their interactions between cells.

Indexed as

Biosensing TechniquesCell Line, TumorCellsHumansMicroscopy, FluorescenceSingle-Cell Analysisadaptationbarcodecell non-autonomous effectfluorescent biosensorKRASlive cell imagingmachine learningmultiplexingreceptor tyrosine kinasesignaling network

Identifiers

PMID34838160
PMCPMC8686192
OpenAlexW3216773365

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.