Evidence map›Paper›PMID 40281337›Full record

ReviewNature protocols2025

Thioether-mediated protein ubiquitination in constructing affinity- and activity-based ubiquitinated protein probes.

Gregory A Davidson, Zeinab Moafian, Amanda R Sensi, Zhihao Zhuang

Abstract readReview
In one paragraph

Review in Nature protocols, 2025. 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

4 authors.

Gregory A Davidson *Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, USA.
Zeinab Moafian *Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, USA.ORCID 0000-0002-9762-4260
Amanda R Sensi *Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, USA.
Zhihao ZhuangDepartment of Chemistry and Biochemistry, University of Delaware, Newark, DE, USA. zzhuang@udel.edu.ORCID 0000-0001-5047-9222

Funding

This renovation project will create over 1455 sq. ft. of state- of-the-art reseaP20GM104316 · NIGMS · UNIVERSITY OF DELAWARE · PI FOX, JOSEPH M · 2014 to 2024
$26.8M
Pilot Research Subproject ProgramP30GM110758 · NIGMS · UNIVERSITY OF DELAWARE · PI POLENOVA, TATYANA · 2014 to 2018
$5.8M
NIH ADMINISTRATIVE SUPPLEMENT AUTOMATED PEPTIDE SYNTHESIZER ZHUANGR01GM129468 · NIGMS · UNIVERSITY OF DELAWARE · PI ZHUANG, ZHIHAO · 2019 to 2022
$1.3M
Deciphering protein ubiquitination with chemical biology toolsR35GM152011 · NIGMS · UNIVERSITY OF DELAWARE · PI Zhihao Zhuang · 2024 to 2026
$1.2M
Investigating autophagic degradation of tau mediated by polyubiquitinationR21AG077189 · NIA · UNIVERSITY OF DELAWARE · PI ZHUANG, ZHIHAO · 2022 to 2022
$424k
NIA NIH HHS R21 AG077189NIGMS NIH HHS P20 GM104316NIGMS NIH HHS P30 GM110758NIGMS NIH HHS R01 GM129468NIGMS NIH HHS R35 GM152011U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM152011U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R21AG077189
6 · The paper itself

Abstract

Protein ubiquitination, a critical regulatory mechanism and post-translational modification in eukaryotic cells, involves the formation of an isopeptide bond between ubiquitin (Ub) and targeted proteins. Despite extensive investigation into the roles played by protein ubiquitination in various cellular processes, many questions remain to be answered. A major challenge in the biochemical and biophysical characterization of protein ubiquitination, along with its associated pathways and protein players, lies in the generation of ubiquitinated proteins, either in mono- or poly-ubiquitinated forms. Enzymatic and chemical strategies have been reported to address this challenge; however, there are still unmet needs for the facile generation of ubiquitinated proteins in the quantity and homogeneity required to precisely decipher the role of various protein-specific ubiquitination events. In this protocol, we provide the ubiquitin research community with a chemical ubiquitination method enabled by an α-bromoketone-mediated ligation strategy. This method can be readily adapted to generate mono- and poly-ubiquitinated proteins of interest through a cysteine introduced to replace the target lysine, with the native cysteines mutated to serine. Using proliferating cell nuclear antigen (PCNA) as an example, we present herein a detailed protocol for generating di- and tri-Ub PCNA that contains a photo-activatable cross-linker for capturing potential reader proteins. The thioether-mediated protein ligation and purification typically takes 2-3 weeks. An important feature of our ubiquitination strategy is the ability to introduce a Michael-acceptor warhead to the linkage, allowing the generation of activity-based probes for deubiquitinases and ubiquitin-carrying enzymes such as HECT and RBR E3 ubiquitin ligases and E2 enzymes. As such, our method is highly versatile and can be readily adapted to investigate the readers and erasers of many proteins that undergo reversible ubiquitination.

Indexed as

SulfidesUbiquitinated ProteinsUbiquitinationHumansProliferating Cell Nuclear AntigenProtein Processing, Post-TranslationalUbiquitinProliferating Cell Nuclear AntigenSulfidesUbiquitinUbiquitinated Proteins

Identifiers

PMID40281337
PMCPMC12611403

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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.