Evidence map›Paper›PMID 27647713›Full record

ArticleAngewandte Chemie (International ed. in English)2016

An Integrated Chemical Cytometry Method: Shining a Light on Akt Activity in Single Cells.

Emilie R Mainz, Qunzhao Wang, David S Lawrence, Nancy L Allbritton

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Optochemical Control of Biological Processes in Cells and Animals.Angewandte Chemie (International ed. in English) · 2018
    Review
  9. Review
  10. 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

4 authors at 1 institution in 1 country.

Emilie R MainzDepartment of Chemistry, University of North Carolina, Chapel Hill, NC, 27599, USA.
Qunzhao WangDepartment of Chemistry, Division of Chemical Biology and Medicinal Chemistry and Department of Pharmacology, University of North Carolina, Chapel Hill, NC, 27599, USA.
David S LawrenceDepartment of Chemistry, Division of Chemical Biology and Medicinal Chemistry and Department of Pharmacology, University of North Carolina, Chapel Hill, NC, 27599, USA.
Nancy L AllbrittonDepartment of Chemistry and Pharmacology, University of North Carolina, Chapel Hill, NC, 27599, USA. nlallbri@unc.edu.ORCID 0000-0002-9242-768X
University of North Carolina at Chapel Hill · US

Funding

SYNTHETIC REGULATORS OF TYROSINE PROTEIN KINASESR01CA079954 · NCI · YESHIVA UNIVERSITY · PI LAWRENCE, DAVID S. · 1999 to 2016
$4.2M
Single-Cell Measurement of Lipid Signaling in Colorectal CancerR01CA177993 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ALLBRITTON, NANCY L. · 2014 to 2018
$3.0M
Single Cell Sampling of Signaling Activity in Triple Negative Breast CancerR01CA203032 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAWRENCE, DAVID S. · 2016 to 2020
$2.4M
NCI NIH HHS R01 CA079954NCI NIH HHS R01 CA177993NCI NIH HHS R01 CA203032
6 · The paper itself

Abstract

Tools to evaluate oncogenic kinase activity in small clinical samples have the power to guide precision medicine in oncology. Existing platforms have demonstrated impressive insights into the activity of protein kinases, but these technologies are unsuitable for the study of kinase behavior in large numbers of primary human cells. To address these limitations, we developed an integrated analysis system that utilizes a light-programmable, cell-permeable reporter deliverable simultaneously to many cells. The reporter's ability to act as a substrate for Akt, a key oncogenic kinase, was masked by a 2-4,5-dimethoxy 2-nitrobenzyl (DMNB) moiety. Upon exposure to ultraviolet light and release of the masking moiety, the substrate sequence enabled programmable reaction times within the cell cytoplasm. When coupled to automated single-cell capillary electrophoresis, statistically significant numbers of primary human cells were readily evaluated for Akt activity.

Indexed as

Biosensing TechniquesFlow CytometrySingle-Cell AnalysisCell Line, TumorHumansProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-aktbiosensorschemical cytometrykinase activity probesphotochemistrysingle-cell analysis

Identifiers

PMID27647713
PMCPMC5149395
OpenAlexW2521123562

What OpenQuestion holds

Textmetadata
LicenceTDM
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.