Evidence map›Paper›PMID 30784263›Full record

ArticleChemical research in toxicology2019

Triphenylphosphonium-Derived Protein Sulfenic Acid Trapping Agents: Synthesis, Reactivity, and Effect on Mitochondrial Function.

Zhe Li, Tom E Forshaw, Reetta J Holmila, Stephen A Vance, Hanzhi Wu, Leslie B Poole, Cristina M Furdui, S Bruce King

Open access · greenAbstract read
In one paragraph

Article in Chemical research in toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  5. Review
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

8 authors at 1 institution in 1 country.

Zhe LiDepartment of Chemistry , Wake Forest University , Winston-Salem , North Carolina 27101 , United States.ORCID 0000-0001-7897-2617
Tom E ForshawDepartment of Internal Medicine , Wake Forest School of Medicine , Winston-Salem , North Carolina 27157 , United States.
Reetta J HolmilaDepartment of Internal Medicine , Wake Forest School of Medicine , Winston-Salem , North Carolina 27157 , United States.
Stephen A VanceDepartment of Chemistry , Wake Forest University , Winston-Salem , North Carolina 27101 , United States.
Hanzhi WuDepartment of Internal Medicine , Wake Forest School of Medicine , Winston-Salem , North Carolina 27157 , United States.
Leslie B PooleDepartment of Biochemistry , Wake Forest School of Medicine , Winston-Salem , North Carolina 27157 , United States.
Cristina M FurduiDepartment of Internal Medicine , Wake Forest School of Medicine , Winston-Salem , North Carolina 27157 , United States.ORCID 0000-0003-3771-7999
S Bruce KingDepartment of Chemistry , Wake Forest University , Winston-Salem , North Carolina 27101 , United States.ORCID 0000-0002-8647-8026
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
New Oxidation-Sensing Probes to Evaluate Mitochondrial Dysfunction in Lung InjuryR33ES025645 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, KING, S BRUCE · 2017 to 2019
$1.5M
New Reagents for Tracking Protein Oxidation in Cells by MS and Imaging MethodsR33CA177461 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2013 to 2015
$1.0M
New Oxidation-Sensing Probes to Evaluate Mitochondrial Dysfunction in Lung InjuryR21ES025645 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, KING, S BRUCE · 2015 to 2016
$428k
NCI NIH HHS P30 CA012197NCI NIH HHS R33 CA177461NIEHS NIH HHS R21 ES025645NIEHS NIH HHS R33 ES025645
6 · The paper itself

Abstract

Redox-mediated protein modifications control numerous processes in both normal and disease metabolism. Protein sulfenic acids, formed from the oxidation of protein cysteine residues, play a critical role in thiol-based redox signaling. The reactivity of protein sulfenic acids requires their identification through chemical trapping, and this paper describes the use of the triphenylphosphonium (TPP) ion to direct known sulfenic acid traps to the mitochondria, a verified source of cellular reactive oxygen species. Coupling of the TPP group with the 2,4-(dioxocyclohexyl)propoxy (DCP) unit and the bicyclo[6.1.0]nonyne (BCN) group produces two new probes, DCP-TPP and BCN-TPP. DCP-TPP and BCN-TPP react with C165A AhpC-SOH, a model protein sulfenic acid, to form the expected adducts with second-order rate constants of k = 1.1 M

Indexed as

A549 CellsHumansMitochondriaMolecular ProbesMolecular StructureOrganophosphorus CompoundsProteinsSulfenic AcidsMolecular ProbesOrganophosphorus CompoundsProteinsSulfenic Acids

Identifiers

PMID30784263
PMCPMC6719313
OpenAlexW2915726625

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.