Evidence map›Paper›PMID 39380184›Full record

ArticleJournal of proteome research2024

Achieving a 35-Plex Tandem Mass Tag Reagent Set through Deuterium Incorporation.

Nathan R Zuniga, Dustin C Frost, Karsten Kuhn, Myungsun Shin, Rebecca L Whitehouse, Ting-Yu Wei, Yuchen He, Shane L Dawson, Ian Pike, Ryan D Bomgarden and 2 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  13. Quantitative Analysis of theBio-protocol · 2025
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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

12 authors.

Nathan R ZunigaDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0001-8718-0638
Dustin C FrostThermo Fisher Scientific, Rockford, Illinois 61101, United States.ORCID 0000-0002-8239-5274
Karsten KuhnProteome Sciences, London KT15 2HJ, U.K.
Myungsun ShinDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.
Rebecca L WhitehouseDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0001-5809-8731
Ting-Yu WeiDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0002-3073-625X
Yuchen HeDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0002-6096-4915
Shane L DawsonDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.
Ian PikeProteome Sciences, London KT15 2HJ, U.K.
Ryan D BomgardenThermo Fisher Scientific, Rockford, Illinois 61101, United States.
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.
Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0002-4291-413X

Funding

New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
Advancing Multiplexed Isobaric Tag-based Strategies for Proteome ProfilingR01GM132129 · NIGMS · HARVARD MEDICAL SCHOOL · PI PAULO, JOAO A · 2019 to 2023
$1.7M
NIGMS NIH HHS R01 GM067945NIGMS NIH HHS R01 GM132129
6 · The paper itself

Abstract

Mass spectrometry-based sample multiplexing with isobaric tags permits the development of high-throughput and precise quantitative biological assays with proteome-wide coverage and minimal missing values. Here, we nearly doubled the multiplexing capability of the TMTpro reagent set to a 35-plex through the incorporation of one deuterium isotope into the reporter group. Substituting deuterium frequently results in suboptimal peak coelution, which can compromise the accuracy of reporter ion-based quantification. To counteract the deuterium effect on quantitation, we implemented a strategy that necessitated the segregation of nondeuterium and deuterium-containing channels into distinct subplexes during normalization procedures, with reassembly through a common bridge channel. This multiplexing strategy of "design independent sub-plexes but acquire together" (DISAT) was used to compare protein expression differences between human cell lines and in a cysteine-profiling (i.e., chemoproteomics) experiment to identify compounds binding to cysteine-113 of Pin1.

Indexed as

DeuteriumProteomicsTandem Mass SpectrometryCysteineHumansIndicators and ReagentsIsotope LabelingNIMA-Interacting Peptidylprolyl IsomeraseProteomeCysteineDeuteriumIndicators and ReagentsNIMA-Interacting Peptidylprolyl IsomerasePIN1 protein, humanProteomeABPPAstraldeuteriumisobaric taggingTMTproTMTproD

Identifiers

PMID39380184
PMCPMC12706455

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.