Evidence map›Paper›PMID 41341063›Full record

ArticleACS central science2025

A Small Molecule Drug-Based Ru(II) Polypyridine Mass-Tag for Multimodal Imaging of Tissue Samples.

Mihyun Park, Melina Rumpf, Guillermo Moreno-Alcántar, Manuel Seiler, Lieby Zborovsky, Katja Steiger, Susanne Kossatz, Angela Casini, Nicole Strittmatter

Abstract read
In one paragraph

Article in ACS central science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Mihyun ParkChair of Medicinal and Bioinorganic Chemistry, Department of Chemistry, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.ORCID https://orcid.org/0000-0002-3665-4247
Melina RumpfChair of Medicinal and Bioinorganic Chemistry, Department of Chemistry, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.
Guillermo Moreno-AlcántarChair of Medicinal and Bioinorganic Chemistry, Department of Chemistry, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.ORCID https://orcid.org/0000-0001-9836-4694
Manuel SeilerCatalysis Research Center Analytic Core Facility, Department of Chemistry, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.
Lieby ZborovskyProfessorship for Analytical Chemistry, Department of Biosciences, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.
Katja SteigerComparative Experimental Pathology, Institute of Pathology, School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.
Susanne KossatzDepartment of Nuclear Medicine, TUM University Hospital, Central Institute for Translational Cancer Research (TranslaTUM), School of Medicine and Health, Technical University of Munich, 81675 Munich, Germany.
Angela CasiniChair of Medicinal and Bioinorganic Chemistry, Department of Chemistry, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.ORCID https://orcid.org/0000-0003-1599-9542
Nicole StrittmatterProfessorship for Analytical Chemistry, Department of Biosciences, School of Natural Sciences, Technical University of Munich, 85748 Garching, Germany.ORCID https://orcid.org/0000-0003-1277-9608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mass spectrometry imaging (MSI) is a powerful tool for spatially resolved multiomics analysis of tissue samples in clinical research. However, its proteomics application is still limited due to challenges such as low ionization efficiency and signal interference from complex tissue environments. On-tissue mass-tag labeling (OTMT) addresses these limitations using affinity-based imaging agents that incorporate cleavable, highly ionizable reporter groups known as mass-tags (MTs). The majority of existing MTs rely on antibodies as targeting elements and organic moieties as reporter groups. Here, we introduce a new class of MTs featuring small-molecule inhibitors as binding motifs. Specifically, we present

Identifiers

PMID41341063
PMCPMC12670285

What OpenQuestion holds

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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.