Evidence map›Paper›PMID 23150405›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2013

Methods for determining protein translocation by the Legionella pneumophila Dot/Icm type IV secretion system.

Wenhan Zhu, Zhao-Qing Luo

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2013. 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

2 authors.

Wenhan ZhuDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.
Zhao-Qing Luo

Funding

Modulation of Host Vesicle Trafficking by Legionella pneumophilaK02AI085403 · NIAID · PURDUE UNIVERSITY · PI LUO, ZHAO-QING · 2010 to 2014
$556k
NIAID NIH HHS K02 AI085403
6 · The paper itself

Abstract

Legionella pneumophila the causative agent of Legionnaires' disease, actively manipulates host cell -processes to establish a membrane-bound replication vacuole permissive for its replication. Establishment of such replication niche requires the Dot/Icm type IV secretion system which translocates a plethora of effectors into host cells. Determining whether a particular protein is a substrate of the transporter is a prerequisite for subsequent functional studies. Thus, a variety of methods have been developed in the last decade to measure Dot/Icm-dependent delivery of protein into the host cell. The combination of these methods and the appropriate screening strategies has allowed for the identification of more than 270 translocated proteins. These efforts have laid a solid foundation for further study of the roles of these proteins in the interactions between L. pneumophila and its host. Here, we summarized the experimental details of these methods.

Indexed as

Bacterial Secretion SystemsAnimalsAntigens, BacterialBacterial ProteinsBacterial Toxinsbeta-LactamasesCell LineFluorescent Antibody TechniqueHumansLegionella pneumophilaProtein Transportanthrax toxinAntigens, BacterialBacterial ProteinsBacterial Secretion SystemsBacterial Toxinsbeta-LactamasesSidC protein, Legionella pneumophila

Identifiers

PMID23150405
PMCPMC11931729

What OpenQuestion holds

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Registered trials

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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.