Evidence map›Paper›PMID 28437088›Full record

ArticleJournal of proteome research2017

HILAQ: A Novel Strategy for Newly Synthesized Protein Quantification.

Yuanhui Ma, Daniel B McClatchy, Salim Barkallah, William W Wood, John R Yates

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. An atlas of ferroptosis-induced secretomes.Cell death and differentiation · 2025
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  12. Proteomic Techniques to Examine Neuronal Translational Dynamics.International journal of molecular sciences · 2019
    Review
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  14. Article
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  18. 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

5 authors at 1 institution in 1 country.

Yuanhui MaDepartment of Chemical Physiology and Molecular and Cellular Neurobiology, The Scripps Research Institute , La Jolla, California 92037, United States.ORCID 0000-0003-0868-3160
Daniel B McClatchyDepartment of Chemical Physiology and Molecular and Cellular Neurobiology, The Scripps Research Institute , La Jolla, California 92037, United States.
Salim BarkallahCambridge Isotope Laboratories, Inc. , 50 Frontage Road, Andover, Massachusetts 01810, United States.
William W WoodCambridge Isotope Laboratories, Inc. , 50 Frontage Road, Andover, Massachusetts 01810, United States.
John R YatesDepartment of Chemical Physiology and Molecular and Cellular Neurobiology, The Scripps Research Institute , La Jolla, California 92037, United States.
Scripps Research Institute · US

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
Proteogenetics of Autism Spectrum DisordersR01MH100175 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI MUOTRI, ALYSSON R., YATES III, JOHN R · 2013 to 2025
$7.4M
Quantitative Proteome Analysis of Brain DevelopmentR01MH067880 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI YATES III, JOHN R · 2003 to 2017
$7.1M
NIGMS NIH HHS P41 GM103533NIMH NIH HHS R01 MH067880NIMH NIH HHS R01 MH100175
6 · The paper itself

Abstract

Here we describe a new strategy, HILAQ (Heavy Isotope Labeled Azidohomoalanine Quantification), to rapidly quantify the molecular vulnerability profile to oxytosis, which is an oxidative stress-induced programed cell death pathway that has been reported to be involved in aging and neurodegenerative diseases. HILAQ was able to quantify 1962 newly synthesized proteins (NSPs) after 1 h of pulse labeling in HEK293T cell line, while 353 proteins were quantified using the previously published QuaNCAT protocol. HILAQ was successfully applied to the HT22 oxytosis model. 226 proteins were found to have a two-fold change in abundance, and 108 proteins were enriched in the cell death pathway, demonstrating the utility of HT22 cells as a tool to study the molecular details of cell death involved in neurodegenerative diseases. The HILAQ strategy simplifies the analysis of newly synthesized proteomes through the use of isobaric labels and achieves higher sensitivity than previously published methods.

Indexed as

Protein BiosynthesisAlanineCell DeathHEK293 CellsHumansIsotope LabelingNeurodegenerative DiseasesOxidative StressProteinsProteomeAlanineazidohomoalanineProteinsProteomeazidohomoalanineheavy isotopeHT22new synthesized proteinsoxytosisproteomics

Identifiers

PMID28437088
PMCPMC5718913
OpenAlexW2950659734

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.