Evidence map›Paper›PMID 19587052›Full record

ArticleJournal of virology2009

Dynamic host energetics and cytoskeletal proteomes in human immunodeficiency virus type 1-infected human primary CD4 cells: analysis by multiplexed label-free mass spectrometry.

Eric Y Chan, Jennifer N Sutton, Jon M Jacobs, Andrey Bondarenko, Richard D Smith, Michael G Katze

Abstract read
In one paragraph

Article in Journal of virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 62 citations in OpenAlex.

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  11. The HIV-1 Vpr Protein: A Multifaceted Target for Therapeutic Intervention.International journal of molecular sciences · 2017
    Review
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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 5 institutions in 1 country.

Eric Y ChanDepartment of Microbiology, University of Washington, Seattle, 98195-8070, USA.
Jennifer N Sutton
Jon M Jacobs
Andrey Bondarenko
Richard D Smith
Michael G Katze
Environmental Molecular Sciences Laboratory · USPacific Northwest National Laboratory · USRosetta Stone (United States) · USThermo Fisher Scientific (United States) · USUniversity of Washington · US

Funding

YILMA SIV VACCINIA VACCINE TRIALP51RR000166 · NCRR · UNIVERSITY OF WASHINGTON · PI CHAMBERLAIN, JEFFREY S · 1985 to 2011
$161.1M
VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
PROTEOMICS COREP30DA015625 · NIDA · UNIVERSITY OF WASHINGTON · PI KATZE, MICHAEL G · 2002 to 2012
$18.9M
DEVELOPMENT OF A PRIMATE GENOMICS RESOURCER24RR016354 · NCRR · UNIVERSITY OF WASHINGTON · PI KATZE, MICHAEL G · 2002 to 2011
$9.7M
DEVELOPMENT OF A PRIMATE GENOMIC RESOURCER24OD011157 · OD · UNIVERSITY OF WASHINGTON · PI KATZE, MICHAEL G · 2012 to 2012
$994k
NCRR NIH HHS P51 RR000166NCRR NIH HHS R24 RR016354NIAID NIH HHS T32 AI007140NIAID NIH HHS T32 AI07140NIDA NIH HHS P30 DA015625NIH HHS R24 OD011157
6 · The paper itself

Abstract

We report on a proteomic analysis of ex vivo human immunodeficiency virus (HIV) type 1 infection in human primary CD4 cells by shotgun liquid chromatography-tandem mass spectrometry analysis, revealing two distinct proteomic profiles at two phases of virus replication. Relative to mock-infected cells, 168 signature proteins exhibited abundance changes at the first sign of Gag p24 production (8 h postinfection [p.i.]) or the peak of virus replication (24 h p.i.); interestingly, most of the changes were exclusive to only one phase of virus replication. Based on characterization by functional ontology and known human-HIV protein interactions, we observed the enrichment for protein abundance increases pertaining to protein synthesis and nucleasomal reorganization amid an otherwise placid cellular proteome at the first sign of HIV replication. In contrast, we observed indications of decreased protein turnover, concomitant with heightened DNA repair activities and preludes to apoptosis, in the presence of robust virus replication. We also observed hints of disruptions in protein and small molecule trafficking. Our label-free proteomic strategy allowed us to perform multiplexed comparisons-we buttressed our detection specificity with the use of a reverse transcriptase inhibitor as a counterscreen, enabling highlighting of cellular protein abundance changes unique to robust virus replication as opposed to viral entry. In conjunction with complementary high-throughput screens for cellular partners of HIV, we put forth a model pinpointing specific rerouting of cellular biosynthetic, energetic, and trafficking pathways as HIV replication accelerates in human primary CD4 cells.

Indexed as

Energy MetabolismCD4-Positive T-LymphocytesCells, CulturedChromatography, LiquidCytoskeletal ProteinsHIV-1HIV InfectionsHumansMetabolic Networks and PathwaysProtein TransportProteomeProteomicsTandem Mass SpectrometryTime FactorsVirus ReplicationCytoskeletal ProteinsProteome

Identifiers

PMID19587052
PMCPMC2738255
OpenAlexW2148406410

What OpenQuestion holds

Textmetadata
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.