Evidence map›Paper›PMID 41835452›Full record

ReviewRSC chemical biology2026

Illuminating microtubule functions with small molecules: past, present and future of fluorescent tubulin-binding probes.

R París-Ogáyar, D Lucena-Agell, K-H Altmann, V Palomo, J F Díaz

Abstract readReview
In one paragraph

Review in RSC chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

R París-OgáyarInstituto Madrileño de Estudios Avanzados en Nanociencia (IMDEA Nanociencia) Madrid Spain valle.palomo@imdea.org.ORCID https://orcid.org/0000-0002-7953-0949
D Lucena-AgellUnit for the Development of Biological, Immunological and Chemical Drugs, Centro de Investigaciones Biológicas Margarita Salas - CSIC Madrid Spain fer@cib.csic.es.ORCID https://orcid.org/0000-0001-7314-8696
K-H AltmannDepartment of Chemistry and Applied Biosciences, ETH Zürich Zürich Switzerland.ORCID https://orcid.org/0000-0002-0747-9734
V PalomoInstituto Madrileño de Estudios Avanzados en Nanociencia (IMDEA Nanociencia) Madrid Spain valle.palomo@imdea.org.ORCID https://orcid.org/0000-0002-1473-4086
J F DíazUnit for the Development of Biological, Immunological and Chemical Drugs, Centro de Investigaciones Biológicas Margarita Salas - CSIC Madrid Spain fer@cib.csic.es.ORCID https://orcid.org/0000-0003-2743-3319

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing tools for the real-time visualization of tubulin, microtubules, and their dynamics is essential for studying key cellular processes such as cell division, migration, and differentiation. In this context, fluorescent small-molecule probes that bind to distinct and specific sites on microtubules have significantly advanced our understanding of tubulin dynamics and functions. In addition, fluorescent probes targeting tubulin have enabled the development of high-throughput screening assays to identify novel anti-tubulin compounds. In this review, we present a comprehensive overview of currently available fluorescent molecules that bind to tubulin, detailing their chemical structures, binding sites, development strategies and relevance to the study of microtubule functions. We also explore future directions in this field and highlight key fluorescent probes that are still lacking. Developing these tools would enable the investigation of tubulin's diverse cellular roles in even greater depth and support the advancement of tubulin-targeted therapeutics.

Identifiers

PMID41835452
PMCPMC12981091

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.