Evidence map›Paper›PMID 23335262›Full record

ArticleChembiochem : a European journal of chemical biology2013

Catch-and-release probes applied to semi-intact cells reveal ubiquitin-specific protease expression in Chlamydia trachomatis infection.

Jasper H L Claessen, Martin D Witte, Nicholas C Yoder, Angela Y Zhu, Eric Spooner, Hidde L Ploegh

Open access · greenAbstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

23 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Synthetic Strategies for Activity-Based Probes to Decode Ubiquitin-Like Modifiers.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Assay Systems for Profiling Deubiquitinating Activity.International journal of molecular sciences · 2020
    Review
  9. Review
  10. Article
  11. The multiple functions of the numerousMicrobial cell (Graz, Austria) · 2019
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Chlamydia cell biology and pathogenesis.Nature reviews. Microbiology · 2016
    Review
  18. Review
  19. Usp12 stabilizes the T-cell receptor complex at the cell surface during signaling.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. Structural basis of substrate recognition by a bacterial deubiquitinase important for dynamics of phagosome ubiquitination.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

6 authors at 1 institution in 1 country.

Jasper H L Claessen *Whitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Martin D Witte *Whitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Nicholas C YoderWhitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Angela Y ZhuWhitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Eric SpoonerWhitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Hidde L PloeghWhitehead Institute for Biomedical Research, 9 Cambridge Center, 02142, Cambridge, MA, USA.
Whitehead Institute for Biomedical Research · US

Funding

Sortase-mediated protein engineering for the study of host-pathogen interactionsR01AI087879 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PLOEGH, HIDDE L. · 2010 to 2019
$4.5M
ASSEMBLY OF MHC CLASS I MOLECULES IN VITRO AND IN VIVOR01AI033456 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PLOEGH, HIDDE L. · 1993 to 2012
$4.0M
NIAID NIH HHS R01 AI033456NIAID NIH HHS R01 AI087879
6 · The paper itself

Abstract

Protein ubiquitylation controls many cellular pathways, and timely removal of ubiquitin by deubiquitylating enzymes (DUBs) is essential to govern these different functions. To map endogenous expression of individual DUBs as well as that of any interacting proteins, we developed a catch-and-release ubiquitin probe. Ubiquitin was equipped with an activity-based warhead and a cleavable linker attached to a biotin affinity-handle through tandem site-specific modification, in which we combined intein chemistry with sortase-mediated ligation. The resulting probe is cell-impermeable and was therefore delivered to the cytosol of perfringolysin O (PFO)-permeabilized cells. This allowed us to retrieve and identify 34 DUBs and their interacting partners. We also noted the expression, in host cells infected with Chlamydia trachomatis, of two additional DUBs. Furthermore, we retrieved and identified chlamydial DUB1 (ChlaDUB1) and DUB2 (ChlaDUB2), demonstrating by experiment that ChlaDUB2, the presence and activity of which had not been detected in infected cells, is in fact expressed during the course of infection.

Indexed as

AminoacyltransferasesAzo CompoundsBacterial ProteinsBacterial ToxinsBiotinChlamydia InfectionsChlamydia trachomatisCysteine EndopeptidasesEndopeptidasesHEK293 CellsHemolysin ProteinsHumansHydrazonesLevulinic AcidsMolecular ProbesUbiquitinAminoacyltransferasesazobenzeneAzo CompoundsBacterial ProteinsBacterial ToxinsBiotinClostridium perfringens theta-toxinCysteine EndopeptidasesEndopeptidasesHemolysin ProteinsHydrazonesLevulinic Acidsmethyl levulinateMolecular Probessortase AUbiquitinUbiquitin-Specific Proteases

Identifiers

PMID23335262
PMCPMC3841013
OpenAlexW2099069541

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.