Evidence map›Paper›PMID 41960701›Full record

ArticleJournal of the American Chemical Society2026

Ribosome Heterogeneity Revealed by Complex-Up Native Mass Spectrometry and Top-Down Proteomics.

Sachin C Tennakoon, Sarah B Giese, Jared B Shaw

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Sachin C TennakoonDepartment of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, United States.ORCID 0009-0002-3751-8631
Sarah B GieseCoe College, Cedar Rapids, Iowa 52402, United States.
Jared B ShawDepartment of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, United States.ORCID 0000-0002-1130-1728

Funding

Targeted mass spectrometry approaches to understand CART processing and recepter interactionsP20GM113126 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI GUO, JIANTAO · 2016 to 2025
$20.8M
Ion laboratory for the elucidation of macromolecular assembly heterogeneityR35GM157097 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI Jared Bryan Shaw · 2025 to 2026
$718k
NIGMS NIH HHS P20 GM113126NIGMS NIH HHS R35 GM157097
6 · The paper itself

Abstract

Characterization of large molecular machines, such as the ribosome, under a breadth of biological states to elucidate regulatory details remains challenging. Herein, a workflow combining complex-up native mass spectrometry (nMS) with infrared multiphoton dissociation (IRMPD) and top-down proteomics (TDP) was developed to enable the rapid and direct characterization of ribosome heterogeneity. Preferential unfolding and fragmentation of rRNA by IRMPD enabled proteoform-resolved characterization of

Indexed as

ProteomicsRibosomal ProteinsRibosomesEscherichia coliMass SpectrometryRibosomal Proteins

Identifiers

PMID41960701
PMCPMC13220301

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.